Other mutations in this stock |
Total: 122 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
T |
3: 137,771,419 (GRCm39) |
R203* |
probably null |
Het |
Abcc2 |
A |
T |
19: 43,795,581 (GRCm39) |
I446F |
probably damaging |
Het |
Afap1l2 |
A |
T |
19: 56,990,699 (GRCm39) |
I18N |
possibly damaging |
Het |
Aida |
A |
T |
1: 183,094,627 (GRCm39) |
E107D |
probably benign |
Het |
Amer2 |
A |
G |
14: 60,617,269 (GRCm39) |
Y362C |
probably damaging |
Het |
Amigo1 |
T |
C |
3: 108,094,644 (GRCm39) |
S48P |
probably benign |
Het |
Ano5 |
A |
G |
7: 51,187,561 (GRCm39) |
K50R |
possibly damaging |
Het |
Anxa2 |
A |
T |
9: 69,391,098 (GRCm39) |
D95V |
probably damaging |
Het |
Arhgap22 |
A |
G |
14: 33,088,916 (GRCm39) |
N466D |
probably damaging |
Het |
Armc3 |
T |
C |
2: 19,297,953 (GRCm39) |
Y575H |
probably damaging |
Het |
Ascc2 |
A |
G |
11: 4,629,257 (GRCm39) |
E523G |
probably benign |
Het |
B3galt5 |
A |
T |
16: 96,117,225 (GRCm39) |
K286M |
probably damaging |
Het |
Bag3 |
C |
T |
7: 128,147,407 (GRCm39) |
H341Y |
probably benign |
Het |
Blm |
G |
T |
7: 80,155,697 (GRCm39) |
|
probably null |
Het |
Cacna1b |
G |
A |
2: 24,622,318 (GRCm39) |
P222L |
probably damaging |
Het |
Cap2 |
T |
A |
13: 46,791,357 (GRCm39) |
Y175N |
possibly damaging |
Het |
Cd81 |
G |
T |
7: 142,620,938 (GRCm39) |
G206* |
probably null |
Het |
Cep290 |
T |
A |
10: 100,367,046 (GRCm39) |
S1132R |
possibly damaging |
Het |
Cluh |
C |
A |
11: 74,550,355 (GRCm39) |
C222* |
probably null |
Het |
Col14a1 |
A |
T |
15: 55,313,336 (GRCm39) |
D1320V |
unknown |
Het |
Col18a1 |
T |
C |
10: 76,916,988 (GRCm39) |
I114V |
unknown |
Het |
Cped1 |
A |
G |
6: 22,233,926 (GRCm39) |
T847A |
probably damaging |
Het |
Cpne7 |
A |
G |
8: 123,854,176 (GRCm39) |
K288E |
possibly damaging |
Het |
Cr2 |
G |
A |
1: 194,836,458 (GRCm39) |
P1278S |
possibly damaging |
Het |
Creb3 |
C |
A |
4: 43,565,327 (GRCm39) |
R202S |
probably damaging |
Het |
Cyp2j9 |
T |
A |
4: 96,460,201 (GRCm39) |
K434M |
probably damaging |
Het |
Dnai3 |
G |
T |
3: 145,769,235 (GRCm39) |
T522K |
possibly damaging |
Het |
Dpp10 |
A |
T |
1: 123,832,833 (GRCm39) |
V48E |
probably null |
Het |
Dsg2 |
A |
G |
18: 20,734,530 (GRCm39) |
K836R |
probably damaging |
Het |
Dst |
A |
G |
1: 34,229,339 (GRCm39) |
T1986A |
probably benign |
Het |
Dvl1 |
G |
A |
4: 155,932,273 (GRCm39) |
V28I |
possibly damaging |
Het |
Ecm2 |
A |
G |
13: 49,683,732 (GRCm39) |
D570G |
probably benign |
Het |
Efhc1 |
T |
A |
1: 21,059,784 (GRCm39) |
C611* |
probably null |
Het |
Epop |
T |
C |
11: 97,519,480 (GRCm39) |
T210A |
probably benign |
Het |
Erc2 |
A |
G |
14: 27,733,593 (GRCm39) |
I556V |
probably benign |
Het |
Fdxacb1 |
A |
T |
9: 50,682,946 (GRCm39) |
N101I |
probably benign |
Het |
Fhad1 |
T |
C |
4: 141,709,473 (GRCm39) |
S294G |
possibly damaging |
Het |
Galnt16 |
A |
G |
12: 80,630,430 (GRCm39) |
D262G |
probably damaging |
Het |
Gorab |
A |
G |
1: 163,224,625 (GRCm39) |
S59P |
probably damaging |
Het |
Gpr161 |
G |
T |
1: 165,134,132 (GRCm39) |
M131I |
probably damaging |
Het |
Gpr22 |
T |
A |
12: 31,759,202 (GRCm39) |
M270L |
probably benign |
Het |
Grin3b |
C |
A |
10: 79,806,746 (GRCm39) |
Q5K |
probably benign |
Het |
Grin3b |
C |
T |
10: 79,810,480 (GRCm39) |
A662V |
probably damaging |
Het |
Gsdmc |
A |
G |
15: 63,673,748 (GRCm39) |
I179T |
probably benign |
Het |
Gsdmc2 |
T |
A |
15: 63,700,086 (GRCm39) |
M229L |
probably benign |
Het |
H2-Eb2 |
A |
G |
17: 34,553,278 (GRCm39) |
I155V |
probably benign |
Het |
Hoga1 |
A |
C |
19: 42,048,459 (GRCm39) |
|
probably null |
Het |
Hs3st5 |
A |
G |
10: 36,708,882 (GRCm39) |
Y139C |
probably damaging |
Het |
Il10ra |
C |
A |
9: 45,167,109 (GRCm39) |
A481S |
probably benign |
Het |
Ints2 |
T |
A |
11: 86,139,760 (GRCm39) |
H278L |
possibly damaging |
Het |
Kalrn |
T |
G |
16: 33,796,108 (GRCm39) |
L1222F |
probably damaging |
Het |
Klhl25 |
T |
A |
7: 75,516,480 (GRCm39) |
V157D |
probably damaging |
Het |
Klk1b26 |
A |
T |
7: 43,666,324 (GRCm39) |
T256S |
probably damaging |
Het |
Krt81 |
T |
C |
15: 101,360,435 (GRCm39) |
Q184R |
probably benign |
Het |
Lce1k |
A |
T |
3: 92,714,125 (GRCm39) |
C20S |
unknown |
Het |
Letm1 |
A |
AG |
5: 33,926,859 (GRCm39) |
|
probably null |
Het |
Lin54 |
A |
G |
5: 100,633,660 (GRCm39) |
|
probably null |
Het |
Lrrc37a |
T |
C |
11: 103,391,087 (GRCm39) |
E1446G |
probably benign |
Het |
Macf1 |
A |
G |
4: 123,350,488 (GRCm39) |
S3792P |
probably damaging |
Het |
Manba |
T |
A |
3: 135,256,952 (GRCm39) |
D538E |
probably benign |
Het |
Mcc |
C |
A |
18: 44,624,382 (GRCm39) |
E213* |
probably null |
Het |
Mfap4 |
T |
C |
11: 61,376,633 (GRCm39) |
|
probably null |
Het |
Muc21 |
A |
T |
17: 35,929,600 (GRCm39) |
S1529T |
probably benign |
Het |
Nebl |
T |
A |
2: 17,457,321 (GRCm39) |
I80F |
probably damaging |
Het |
Nek4 |
A |
G |
14: 30,678,910 (GRCm39) |
I145V |
probably damaging |
Het |
Nlrp14 |
T |
C |
7: 106,795,407 (GRCm39) |
V230A |
probably benign |
Het |
Nxf3 |
G |
A |
X: 134,976,583 (GRCm39) |
P380S |
possibly damaging |
Het |
Or11h6 |
G |
A |
14: 50,880,323 (GRCm39) |
C195Y |
possibly damaging |
Het |
Or1a1 |
T |
C |
11: 74,086,989 (GRCm39) |
V220A |
probably damaging |
Het |
Or5b99 |
T |
C |
19: 12,976,866 (GRCm39) |
V172A |
possibly damaging |
Het |
Or5p66 |
C |
A |
7: 107,885,566 (GRCm39) |
G256* |
probably null |
Het |
Or6k8-ps1 |
C |
T |
1: 173,979,687 (GRCm39) |
H202Y |
probably damaging |
Het |
Pcdhb13 |
C |
T |
18: 37,576,912 (GRCm39) |
T430I |
possibly damaging |
Het |
Piezo2 |
A |
T |
18: 63,207,733 (GRCm39) |
L1426Q |
probably null |
Het |
Pigk |
T |
A |
3: 152,450,131 (GRCm39) |
Y212N |
probably damaging |
Het |
Pigm |
T |
G |
1: 172,204,828 (GRCm39) |
L188R |
probably damaging |
Het |
Plce1 |
T |
C |
19: 38,766,368 (GRCm39) |
F2117S |
probably damaging |
Het |
Plec |
A |
G |
15: 76,057,743 (GRCm39) |
F4055L |
probably damaging |
Het |
Plk5 |
C |
T |
10: 80,198,936 (GRCm39) |
S435L |
possibly damaging |
Het |
Pms1 |
G |
A |
1: 53,321,201 (GRCm39) |
L11F |
probably damaging |
Het |
Prl3b1 |
C |
T |
13: 27,431,895 (GRCm39) |
T140I |
possibly damaging |
Het |
Prl7a1 |
T |
G |
13: 27,817,655 (GRCm39) |
D203A |
probably damaging |
Het |
Psg17 |
A |
G |
7: 18,548,577 (GRCm39) |
V398A |
probably benign |
Het |
Pum1 |
T |
A |
4: 130,445,529 (GRCm39) |
I166K |
possibly damaging |
Het |
R3hdm1 |
T |
A |
1: 128,096,753 (GRCm39) |
D108E |
probably damaging |
Het |
Reln |
A |
T |
5: 22,174,358 (GRCm39) |
D1948E |
possibly damaging |
Het |
Rnf112 |
C |
T |
11: 61,343,252 (GRCm39) |
R141Q |
probably damaging |
Het |
Rnf145 |
T |
C |
11: 44,452,293 (GRCm39) |
V424A |
possibly damaging |
Het |
Serpina3m |
C |
A |
12: 104,355,958 (GRCm39) |
Y208* |
probably null |
Het |
Serpind1 |
T |
C |
16: 17,160,808 (GRCm39) |
V446A |
probably benign |
Het |
Shc3 |
T |
A |
13: 51,596,872 (GRCm39) |
M384L |
probably benign |
Het |
Slc38a11 |
A |
G |
2: 65,160,683 (GRCm39) |
F304L |
probably benign |
Het |
Slpi |
C |
T |
2: 164,197,463 (GRCm39) |
C28Y |
probably damaging |
Het |
Specc1 |
C |
A |
11: 61,920,120 (GRCm39) |
P7T |
possibly damaging |
Het |
Spib |
T |
C |
7: 44,178,281 (GRCm39) |
E180G |
probably benign |
Het |
Spint5 |
T |
C |
2: 164,558,903 (GRCm39) |
|
probably benign |
Het |
Ssr2 |
T |
A |
3: 88,484,174 (GRCm39) |
|
probably benign |
Het |
Tbrg1 |
T |
C |
9: 37,560,715 (GRCm39) |
D387G |
probably benign |
Het |
Tex14 |
T |
G |
11: 87,440,296 (GRCm39) |
L1367R |
probably damaging |
Het |
Tfpi |
A |
C |
2: 84,288,360 (GRCm39) |
|
probably benign |
Het |
Tlr5 |
T |
A |
1: 182,801,912 (GRCm39) |
D405E |
probably damaging |
Het |
Tnnt3 |
C |
T |
7: 142,065,262 (GRCm39) |
R131C |
possibly damaging |
Het |
Tpx2 |
T |
A |
2: 152,732,544 (GRCm39) |
M606K |
probably benign |
Het |
Trim30a |
T |
A |
7: 104,079,437 (GRCm39) |
|
probably benign |
Het |
Trim46 |
A |
T |
3: 89,145,008 (GRCm39) |
Y489N |
probably damaging |
Het |
Trpm6 |
A |
T |
19: 18,773,648 (GRCm39) |
H380L |
probably benign |
Het |
Tstd2 |
A |
G |
4: 46,120,563 (GRCm39) |
I279T |
probably benign |
Het |
Ttn |
C |
T |
2: 76,776,735 (GRCm39) |
|
probably null |
Het |
Txnl1 |
T |
C |
18: 63,812,585 (GRCm39) |
T70A |
probably benign |
Het |
Ush2a |
C |
T |
1: 188,310,729 (GRCm39) |
|
probably benign |
Het |
Usp1 |
A |
G |
4: 98,822,531 (GRCm39) |
D615G |
probably benign |
Het |
Virma |
T |
A |
4: 11,519,242 (GRCm39) |
C830S |
probably benign |
Het |
Vmn1r7 |
A |
T |
6: 57,001,853 (GRCm39) |
S136T |
probably benign |
Het |
Vmn2r9 |
A |
G |
5: 108,994,305 (GRCm39) |
V448A |
probably damaging |
Het |
Vps11 |
G |
A |
9: 44,270,524 (GRCm39) |
H183Y |
probably damaging |
Het |
Vsig10l |
A |
G |
7: 43,116,892 (GRCm39) |
T476A |
possibly damaging |
Het |
Whamm |
C |
T |
7: 81,241,519 (GRCm39) |
R277* |
probably null |
Het |
Wnt8a |
A |
G |
18: 34,677,937 (GRCm39) |
D115G |
probably damaging |
Het |
Xndc1 |
T |
A |
7: 101,722,398 (GRCm39) |
V21E |
probably damaging |
Het |
Zc3hav1 |
C |
A |
6: 38,313,452 (GRCm39) |
V198L |
probably damaging |
Het |
Zfp874a |
T |
A |
13: 67,590,623 (GRCm39) |
I354F |
probably benign |
Het |
Zfr2 |
A |
T |
10: 81,078,686 (GRCm39) |
D306V |
possibly damaging |
Het |
|
Other mutations in Tnxb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Tnxb
|
APN |
17 |
34,904,603 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00424:Tnxb
|
APN |
17 |
34,933,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00486:Tnxb
|
APN |
17 |
34,911,356 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00952:Tnxb
|
APN |
17 |
34,932,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00974:Tnxb
|
APN |
17 |
34,937,707 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01017:Tnxb
|
APN |
17 |
34,912,782 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01082:Tnxb
|
APN |
17 |
34,933,584 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01397:Tnxb
|
APN |
17 |
34,933,647 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01473:Tnxb
|
APN |
17 |
34,904,675 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01642:Tnxb
|
APN |
17 |
34,937,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01774:Tnxb
|
APN |
17 |
34,907,813 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01971:Tnxb
|
APN |
17 |
34,891,271 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02016:Tnxb
|
APN |
17 |
34,891,249 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02160:Tnxb
|
APN |
17 |
34,933,719 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02473:Tnxb
|
APN |
17 |
34,936,736 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Tnxb
|
APN |
17 |
34,903,913 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02831:Tnxb
|
APN |
17 |
34,922,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02838:Tnxb
|
APN |
17 |
34,908,606 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02965:Tnxb
|
APN |
17 |
34,928,628 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03155:Tnxb
|
APN |
17 |
34,932,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03194:Tnxb
|
APN |
17 |
34,914,921 (GRCm39) |
nonsense |
probably null |
|
IGL03215:Tnxb
|
APN |
17 |
34,911,499 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03256:Tnxb
|
APN |
17 |
34,907,694 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Tnxb
|
UTSW |
17 |
34,907,672 (GRCm39) |
missense |
probably damaging |
1.00 |
BB018:Tnxb
|
UTSW |
17 |
34,907,672 (GRCm39) |
missense |
probably damaging |
1.00 |
E0370:Tnxb
|
UTSW |
17 |
34,897,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Tnxb
|
UTSW |
17 |
34,901,266 (GRCm39) |
missense |
probably benign |
0.07 |
R0049:Tnxb
|
UTSW |
17 |
34,928,542 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0050:Tnxb
|
UTSW |
17 |
34,892,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Tnxb
|
UTSW |
17 |
34,918,007 (GRCm39) |
missense |
probably benign |
0.32 |
R0233:Tnxb
|
UTSW |
17 |
34,918,007 (GRCm39) |
missense |
probably benign |
0.32 |
R0311:Tnxb
|
UTSW |
17 |
34,935,958 (GRCm39) |
missense |
probably damaging |
0.97 |
R0326:Tnxb
|
UTSW |
17 |
34,917,153 (GRCm39) |
missense |
probably benign |
0.32 |
R0387:Tnxb
|
UTSW |
17 |
34,902,548 (GRCm39) |
missense |
probably benign |
0.30 |
R0396:Tnxb
|
UTSW |
17 |
34,890,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R0511:Tnxb
|
UTSW |
17 |
34,937,219 (GRCm39) |
missense |
probably damaging |
0.96 |
R0540:Tnxb
|
UTSW |
17 |
34,890,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R0563:Tnxb
|
UTSW |
17 |
34,935,921 (GRCm39) |
missense |
probably benign |
0.05 |
R0575:Tnxb
|
UTSW |
17 |
34,936,180 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0586:Tnxb
|
UTSW |
17 |
34,891,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Tnxb
|
UTSW |
17 |
34,890,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R0622:Tnxb
|
UTSW |
17 |
34,937,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Tnxb
|
UTSW |
17 |
34,902,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R0709:Tnxb
|
UTSW |
17 |
34,908,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R0898:Tnxb
|
UTSW |
17 |
34,889,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R0970:Tnxb
|
UTSW |
17 |
34,917,917 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0972:Tnxb
|
UTSW |
17 |
34,904,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R1118:Tnxb
|
UTSW |
17 |
34,904,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1119:Tnxb
|
UTSW |
17 |
34,904,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1226:Tnxb
|
UTSW |
17 |
34,907,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R1296:Tnxb
|
UTSW |
17 |
34,890,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1297:Tnxb
|
UTSW |
17 |
34,929,140 (GRCm39) |
missense |
probably damaging |
0.96 |
R1349:Tnxb
|
UTSW |
17 |
34,929,267 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1356:Tnxb
|
UTSW |
17 |
34,914,446 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1372:Tnxb
|
UTSW |
17 |
34,929,267 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1521:Tnxb
|
UTSW |
17 |
34,930,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Tnxb
|
UTSW |
17 |
34,937,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Tnxb
|
UTSW |
17 |
34,929,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R1735:Tnxb
|
UTSW |
17 |
34,936,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Tnxb
|
UTSW |
17 |
34,902,548 (GRCm39) |
missense |
probably benign |
0.30 |
R1802:Tnxb
|
UTSW |
17 |
34,922,863 (GRCm39) |
missense |
probably damaging |
0.98 |
R1824:Tnxb
|
UTSW |
17 |
34,911,307 (GRCm39) |
nonsense |
probably null |
|
R1838:Tnxb
|
UTSW |
17 |
34,897,884 (GRCm39) |
missense |
probably damaging |
0.96 |
R1863:Tnxb
|
UTSW |
17 |
34,889,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Tnxb
|
UTSW |
17 |
34,922,431 (GRCm39) |
nonsense |
probably null |
|
R1867:Tnxb
|
UTSW |
17 |
34,890,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R1883:Tnxb
|
UTSW |
17 |
34,908,539 (GRCm39) |
missense |
probably benign |
0.01 |
R1884:Tnxb
|
UTSW |
17 |
34,908,539 (GRCm39) |
missense |
probably benign |
0.01 |
R1889:Tnxb
|
UTSW |
17 |
34,914,799 (GRCm39) |
missense |
probably damaging |
0.97 |
R1969:Tnxb
|
UTSW |
17 |
34,898,055 (GRCm39) |
missense |
probably benign |
0.20 |
R1989:Tnxb
|
UTSW |
17 |
34,912,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R1989:Tnxb
|
UTSW |
17 |
34,902,351 (GRCm39) |
missense |
probably benign |
0.08 |
R1991:Tnxb
|
UTSW |
17 |
34,901,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R1992:Tnxb
|
UTSW |
17 |
34,890,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R2001:Tnxb
|
UTSW |
17 |
34,911,553 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2018:Tnxb
|
UTSW |
17 |
34,890,724 (GRCm39) |
missense |
probably benign |
0.04 |
R2030:Tnxb
|
UTSW |
17 |
34,937,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Tnxb
|
UTSW |
17 |
34,918,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R2103:Tnxb
|
UTSW |
17 |
34,901,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R2116:Tnxb
|
UTSW |
17 |
34,891,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Tnxb
|
UTSW |
17 |
34,928,391 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2207:Tnxb
|
UTSW |
17 |
34,928,391 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2215:Tnxb
|
UTSW |
17 |
34,923,114 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2413:Tnxb
|
UTSW |
17 |
34,937,252 (GRCm39) |
missense |
probably damaging |
0.99 |
R2680:Tnxb
|
UTSW |
17 |
34,922,594 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2910:Tnxb
|
UTSW |
17 |
34,891,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R2984:Tnxb
|
UTSW |
17 |
34,897,636 (GRCm39) |
nonsense |
probably null |
|
R3120:Tnxb
|
UTSW |
17 |
34,911,329 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3429:Tnxb
|
UTSW |
17 |
34,922,561 (GRCm39) |
missense |
probably damaging |
0.98 |
R3429:Tnxb
|
UTSW |
17 |
34,891,605 (GRCm39) |
nonsense |
probably null |
|
R3552:Tnxb
|
UTSW |
17 |
34,937,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R3698:Tnxb
|
UTSW |
17 |
34,909,407 (GRCm39) |
critical splice donor site |
probably null |
|
R3720:Tnxb
|
UTSW |
17 |
34,931,938 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3841:Tnxb
|
UTSW |
17 |
34,917,897 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3848:Tnxb
|
UTSW |
17 |
34,909,369 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3886:Tnxb
|
UTSW |
17 |
34,937,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R4074:Tnxb
|
UTSW |
17 |
34,890,845 (GRCm39) |
missense |
probably benign |
0.22 |
R4159:Tnxb
|
UTSW |
17 |
34,930,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R4160:Tnxb
|
UTSW |
17 |
34,930,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R4161:Tnxb
|
UTSW |
17 |
34,930,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R4181:Tnxb
|
UTSW |
17 |
34,928,428 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4210:Tnxb
|
UTSW |
17 |
34,929,951 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4275:Tnxb
|
UTSW |
17 |
34,917,205 (GRCm39) |
missense |
probably damaging |
0.98 |
R4329:Tnxb
|
UTSW |
17 |
34,912,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R4394:Tnxb
|
UTSW |
17 |
34,897,636 (GRCm39) |
nonsense |
probably null |
|
R4395:Tnxb
|
UTSW |
17 |
34,897,636 (GRCm39) |
nonsense |
probably null |
|
R4397:Tnxb
|
UTSW |
17 |
34,897,636 (GRCm39) |
nonsense |
probably null |
|
R4540:Tnxb
|
UTSW |
17 |
34,922,309 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4673:Tnxb
|
UTSW |
17 |
34,891,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R4719:Tnxb
|
UTSW |
17 |
34,908,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Tnxb
|
UTSW |
17 |
34,918,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R4753:Tnxb
|
UTSW |
17 |
34,914,909 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4777:Tnxb
|
UTSW |
17 |
34,890,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Tnxb
|
UTSW |
17 |
34,936,981 (GRCm39) |
missense |
probably damaging |
0.98 |
R4898:Tnxb
|
UTSW |
17 |
34,914,566 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4938:Tnxb
|
UTSW |
17 |
34,932,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R5044:Tnxb
|
UTSW |
17 |
34,936,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R5100:Tnxb
|
UTSW |
17 |
34,929,902 (GRCm39) |
missense |
probably damaging |
0.99 |
R5223:Tnxb
|
UTSW |
17 |
34,923,052 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5269:Tnxb
|
UTSW |
17 |
34,922,582 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5333:Tnxb
|
UTSW |
17 |
34,909,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R5454:Tnxb
|
UTSW |
17 |
34,928,599 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5470:Tnxb
|
UTSW |
17 |
34,935,947 (GRCm39) |
missense |
probably null |
1.00 |
R5475:Tnxb
|
UTSW |
17 |
34,908,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Tnxb
|
UTSW |
17 |
34,929,998 (GRCm39) |
missense |
probably benign |
|
R5596:Tnxb
|
UTSW |
17 |
34,907,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R5599:Tnxb
|
UTSW |
17 |
34,909,179 (GRCm39) |
missense |
probably benign |
0.22 |
R5599:Tnxb
|
UTSW |
17 |
34,909,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R5615:Tnxb
|
UTSW |
17 |
34,902,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R5620:Tnxb
|
UTSW |
17 |
34,936,504 (GRCm39) |
nonsense |
probably null |
|
R5625:Tnxb
|
UTSW |
17 |
34,904,185 (GRCm39) |
missense |
probably benign |
0.30 |
R5734:Tnxb
|
UTSW |
17 |
34,917,884 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5896:Tnxb
|
UTSW |
17 |
34,891,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R5961:Tnxb
|
UTSW |
17 |
34,937,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R5974:Tnxb
|
UTSW |
17 |
34,904,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Tnxb
|
UTSW |
17 |
34,929,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R6134:Tnxb
|
UTSW |
17 |
34,890,986 (GRCm39) |
missense |
probably damaging |
0.96 |
R6325:Tnxb
|
UTSW |
17 |
34,911,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6358:Tnxb
|
UTSW |
17 |
34,897,968 (GRCm39) |
missense |
probably damaging |
0.98 |
R6362:Tnxb
|
UTSW |
17 |
34,913,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R6432:Tnxb
|
UTSW |
17 |
34,936,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R6461:Tnxb
|
UTSW |
17 |
34,890,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R6467:Tnxb
|
UTSW |
17 |
34,912,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Tnxb
|
UTSW |
17 |
34,909,166 (GRCm39) |
missense |
probably damaging |
0.98 |
R6477:Tnxb
|
UTSW |
17 |
34,938,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R6631:Tnxb
|
UTSW |
17 |
34,937,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:Tnxb
|
UTSW |
17 |
34,928,606 (GRCm39) |
nonsense |
probably null |
|
R6787:Tnxb
|
UTSW |
17 |
34,929,710 (GRCm39) |
missense |
probably benign |
0.02 |
R6805:Tnxb
|
UTSW |
17 |
34,917,127 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6860:Tnxb
|
UTSW |
17 |
34,932,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R6883:Tnxb
|
UTSW |
17 |
34,937,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R7049:Tnxb
|
UTSW |
17 |
34,936,242 (GRCm39) |
critical splice donor site |
probably null |
|
R7107:Tnxb
|
UTSW |
17 |
34,890,314 (GRCm39) |
missense |
unknown |
|
R7172:Tnxb
|
UTSW |
17 |
34,914,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R7206:Tnxb
|
UTSW |
17 |
34,923,075 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7219:Tnxb
|
UTSW |
17 |
34,898,039 (GRCm39) |
missense |
probably benign |
0.08 |
R7237:Tnxb
|
UTSW |
17 |
34,901,170 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7257:Tnxb
|
UTSW |
17 |
34,935,475 (GRCm39) |
missense |
probably benign |
0.44 |
R7269:Tnxb
|
UTSW |
17 |
34,914,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R7302:Tnxb
|
UTSW |
17 |
34,897,875 (GRCm39) |
missense |
probably benign |
0.41 |
R7372:Tnxb
|
UTSW |
17 |
34,936,228 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7384:Tnxb
|
UTSW |
17 |
34,937,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Tnxb
|
UTSW |
17 |
34,937,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R7449:Tnxb
|
UTSW |
17 |
34,922,335 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7480:Tnxb
|
UTSW |
17 |
34,934,747 (GRCm39) |
missense |
probably damaging |
0.96 |
R7506:Tnxb
|
UTSW |
17 |
34,934,665 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7586:Tnxb
|
UTSW |
17 |
34,935,382 (GRCm39) |
missense |
probably damaging |
0.98 |
R7688:Tnxb
|
UTSW |
17 |
34,890,880 (GRCm39) |
missense |
probably benign |
0.23 |
R7690:Tnxb
|
UTSW |
17 |
34,908,494 (GRCm39) |
missense |
probably benign |
0.03 |
R7690:Tnxb
|
UTSW |
17 |
34,908,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R7732:Tnxb
|
UTSW |
17 |
34,913,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R7735:Tnxb
|
UTSW |
17 |
34,890,398 (GRCm39) |
missense |
unknown |
|
R7760:Tnxb
|
UTSW |
17 |
34,931,911 (GRCm39) |
missense |
probably damaging |
0.96 |
R7874:Tnxb
|
UTSW |
17 |
34,930,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R7909:Tnxb
|
UTSW |
17 |
34,911,428 (GRCm39) |
missense |
probably benign |
0.02 |
R7922:Tnxb
|
UTSW |
17 |
34,933,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7931:Tnxb
|
UTSW |
17 |
34,907,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7949:Tnxb
|
UTSW |
17 |
34,936,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R7953:Tnxb
|
UTSW |
17 |
34,929,077 (GRCm39) |
missense |
probably benign |
0.03 |
R7953:Tnxb
|
UTSW |
17 |
34,928,509 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7977:Tnxb
|
UTSW |
17 |
34,929,194 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7985:Tnxb
|
UTSW |
17 |
34,935,984 (GRCm39) |
critical splice donor site |
probably null |
|
R7987:Tnxb
|
UTSW |
17 |
34,929,194 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8040:Tnxb
|
UTSW |
17 |
34,935,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Tnxb
|
UTSW |
17 |
34,923,153 (GRCm39) |
missense |
probably damaging |
0.98 |
R8074:Tnxb
|
UTSW |
17 |
34,922,955 (GRCm39) |
missense |
probably benign |
0.32 |
R8089:Tnxb
|
UTSW |
17 |
34,891,763 (GRCm39) |
missense |
unknown |
|
R8169:Tnxb
|
UTSW |
17 |
34,918,181 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8348:Tnxb
|
UTSW |
17 |
34,929,102 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8352:Tnxb
|
UTSW |
17 |
34,908,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R8362:Tnxb
|
UTSW |
17 |
34,931,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R8452:Tnxb
|
UTSW |
17 |
34,908,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R8527:Tnxb
|
UTSW |
17 |
34,907,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R8754:Tnxb
|
UTSW |
17 |
34,934,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R8813:Tnxb
|
UTSW |
17 |
34,938,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R8936:Tnxb
|
UTSW |
17 |
34,904,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R8986:Tnxb
|
UTSW |
17 |
34,897,646 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9001:Tnxb
|
UTSW |
17 |
34,922,410 (GRCm39) |
missense |
probably benign |
0.32 |
R9215:Tnxb
|
UTSW |
17 |
34,891,564 (GRCm39) |
missense |
unknown |
|
R9226:Tnxb
|
UTSW |
17 |
34,904,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R9276:Tnxb
|
UTSW |
17 |
34,929,134 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9279:Tnxb
|
UTSW |
17 |
34,898,088 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9363:Tnxb
|
UTSW |
17 |
34,917,294 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9367:Tnxb
|
UTSW |
17 |
34,931,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R9494:Tnxb
|
UTSW |
17 |
34,904,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R9606:Tnxb
|
UTSW |
17 |
34,914,578 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9650:Tnxb
|
UTSW |
17 |
34,930,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R9677:Tnxb
|
UTSW |
17 |
34,917,878 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9690:Tnxb
|
UTSW |
17 |
34,936,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Tnxb
|
UTSW |
17 |
34,903,987 (GRCm39) |
missense |
probably benign |
0.32 |
X0004:Tnxb
|
UTSW |
17 |
34,922,389 (GRCm39) |
missense |
possibly damaging |
0.71 |
X0010:Tnxb
|
UTSW |
17 |
34,890,908 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Tnxb
|
UTSW |
17 |
34,913,163 (GRCm39) |
missense |
possibly damaging |
0.51 |
X0063:Tnxb
|
UTSW |
17 |
34,922,482 (GRCm39) |
missense |
probably damaging |
0.98 |
X0064:Tnxb
|
UTSW |
17 |
34,913,006 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tnxb
|
UTSW |
17 |
34,937,700 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Tnxb
|
UTSW |
17 |
34,902,305 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tnxb
|
UTSW |
17 |
34,890,740 (GRCm39) |
missense |
unknown |
|
|