Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
A |
T |
7: 130,945,431 (GRCm39) |
Y401* |
probably null |
Het |
4932415M13Rik |
C |
A |
17: 54,032,065 (GRCm39) |
|
noncoding transcript |
Het |
Abtb3 |
A |
G |
10: 85,223,248 (GRCm39) |
D19G |
unknown |
Het |
Acoxl |
T |
A |
2: 127,820,692 (GRCm39) |
S81R |
probably damaging |
Het |
Adamtsl4 |
A |
G |
3: 95,584,924 (GRCm39) |
C915R |
probably damaging |
Het |
Adgra3 |
C |
T |
5: 50,164,117 (GRCm39) |
M287I |
probably benign |
Het |
Afg1l |
T |
G |
10: 42,276,395 (GRCm39) |
D250A |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Amfr |
T |
C |
8: 94,700,871 (GRCm39) |
T530A |
probably benign |
Het |
Ank2 |
C |
T |
3: 126,723,415 (GRCm39) |
V971M |
probably damaging |
Het |
App |
A |
G |
16: 84,762,656 (GRCm39) |
S656P |
probably damaging |
Het |
Arid5a |
T |
A |
1: 36,358,656 (GRCm39) |
|
probably null |
Het |
Asic5 |
T |
A |
3: 81,907,029 (GRCm39) |
V60D |
possibly damaging |
Het |
Atm |
G |
T |
9: 53,412,000 (GRCm39) |
H1019N |
probably benign |
Het |
Cep250 |
A |
G |
2: 155,807,466 (GRCm39) |
K277R |
probably benign |
Het |
Chrna7 |
C |
T |
7: 62,749,255 (GRCm39) |
R409H |
probably damaging |
Het |
Chrng |
A |
T |
1: 87,138,628 (GRCm39) |
N419I |
possibly damaging |
Het |
Ciao1 |
T |
C |
2: 127,087,739 (GRCm39) |
S199G |
probably benign |
Het |
Clstn2 |
A |
T |
9: 97,340,290 (GRCm39) |
M694K |
possibly damaging |
Het |
Cpeb2 |
A |
G |
5: 43,391,181 (GRCm39) |
|
probably benign |
Het |
Cyp2c69 |
T |
A |
19: 39,864,810 (GRCm39) |
I223F |
probably benign |
Het |
Dennd1b |
A |
T |
1: 139,097,492 (GRCm39) |
|
probably null |
Het |
Dnah17 |
A |
T |
11: 117,917,575 (GRCm39) |
L4162Q |
probably damaging |
Het |
Dnm1 |
T |
C |
2: 32,213,463 (GRCm39) |
M506V |
probably benign |
Het |
Ecsit |
A |
G |
9: 21,986,107 (GRCm39) |
V173A |
probably damaging |
Het |
Fam13b |
T |
C |
18: 34,584,492 (GRCm39) |
|
probably null |
Het |
Fgl2 |
T |
A |
5: 21,577,730 (GRCm39) |
W6R |
possibly damaging |
Het |
Galnt9 |
G |
A |
5: 110,767,038 (GRCm39) |
R503H |
probably damaging |
Het |
Gramd1a |
C |
T |
7: 30,838,959 (GRCm39) |
V247M |
possibly damaging |
Het |
Grip2 |
A |
T |
6: 91,754,379 (GRCm39) |
I632N |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,286,462 (GRCm39) |
V3627A |
probably damaging |
Het |
Ipo8 |
T |
C |
6: 148,691,390 (GRCm39) |
Y660C |
probably benign |
Het |
Isg15 |
T |
C |
4: 156,284,265 (GRCm39) |
R88G |
possibly damaging |
Het |
Itgb5 |
T |
A |
16: 33,730,870 (GRCm39) |
D388E |
probably benign |
Het |
Jhy |
T |
C |
9: 40,856,133 (GRCm39) |
Y118C |
probably damaging |
Het |
Kalrn |
G |
A |
16: 34,025,696 (GRCm39) |
T931M |
probably damaging |
Het |
Kif21a |
A |
G |
15: 90,833,250 (GRCm39) |
|
probably null |
Het |
Lama2 |
A |
T |
10: 27,142,667 (GRCm39) |
Y604N |
probably damaging |
Het |
Lrp3 |
T |
G |
7: 34,912,586 (GRCm39) |
S34R |
possibly damaging |
Het |
Lrrc37 |
C |
T |
11: 103,431,700 (GRCm39) |
V1372I |
probably benign |
Het |
Lyn |
T |
C |
4: 3,738,867 (GRCm39) |
|
probably null |
Het |
Mroh8 |
C |
T |
2: 157,113,896 (GRCm39) |
V132I |
probably benign |
Het |
Mthfd1l |
T |
C |
10: 4,098,093 (GRCm39) |
F977L |
probably damaging |
Het |
Nol8 |
C |
T |
13: 49,820,933 (GRCm39) |
T912M |
possibly damaging |
Het |
Nrxn1 |
A |
T |
17: 90,515,845 (GRCm39) |
N169K |
probably damaging |
Het |
Oplah |
A |
G |
15: 76,180,867 (GRCm39) |
Y1279H |
probably benign |
Het |
Or10ag56 |
T |
C |
2: 87,139,754 (GRCm39) |
V207A |
probably benign |
Het |
Or4c101 |
T |
A |
2: 88,390,599 (GRCm39) |
M262K |
possibly damaging |
Het |
Pcsk5 |
T |
C |
19: 17,729,458 (GRCm39) |
N129S |
probably benign |
Het |
Pcyt2 |
G |
T |
11: 120,503,894 (GRCm39) |
P185T |
probably benign |
Het |
Pdlim2 |
A |
G |
14: 70,411,784 (GRCm39) |
|
probably null |
Het |
Pgs1 |
T |
C |
11: 117,905,554 (GRCm39) |
|
probably benign |
Het |
Qprt |
A |
G |
7: 126,707,343 (GRCm39) |
V251A |
probably benign |
Het |
Rasal2 |
A |
C |
1: 156,985,170 (GRCm39) |
L834R |
probably damaging |
Het |
Reg1 |
T |
C |
6: 78,405,432 (GRCm39) |
C161R |
probably damaging |
Het |
S1pr5 |
T |
C |
9: 21,155,346 (GRCm39) |
D360G |
possibly damaging |
Het |
Sart3 |
C |
A |
5: 113,890,280 (GRCm39) |
V482F |
probably benign |
Het |
Scarf2 |
A |
G |
16: 17,620,713 (GRCm39) |
E127G |
probably damaging |
Het |
Serinc5 |
T |
C |
13: 92,825,305 (GRCm39) |
S245P |
probably damaging |
Het |
Serpinc1 |
G |
T |
1: 160,821,087 (GRCm39) |
R57L |
probably damaging |
Het |
Setd2 |
A |
G |
9: 110,378,932 (GRCm39) |
S632G |
probably benign |
Het |
Sgca |
A |
T |
11: 94,860,217 (GRCm39) |
L307M |
probably damaging |
Het |
Slc7a9 |
C |
A |
7: 35,154,000 (GRCm39) |
Q208K |
probably benign |
Het |
Slfn10-ps |
C |
T |
11: 82,920,869 (GRCm39) |
|
noncoding transcript |
Het |
Spam1 |
A |
T |
6: 24,796,256 (GRCm39) |
D69V |
probably damaging |
Het |
Tanc1 |
A |
G |
2: 59,673,365 (GRCm39) |
E1490G |
probably benign |
Het |
Tbc1d22a |
G |
T |
15: 86,123,416 (GRCm39) |
D150Y |
probably benign |
Het |
Tex10 |
C |
T |
4: 48,456,800 (GRCm39) |
R637Q |
probably benign |
Het |
Tlx1 |
A |
G |
19: 45,144,443 (GRCm39) |
D55G |
possibly damaging |
Het |
Tram2 |
G |
T |
1: 21,074,458 (GRCm39) |
N241K |
probably damaging |
Het |
Ttc23l |
T |
C |
15: 10,523,744 (GRCm39) |
Y325C |
probably damaging |
Het |
Ubac2 |
T |
A |
14: 122,142,582 (GRCm39) |
S27T |
probably benign |
Het |
Utrn |
G |
A |
10: 12,603,473 (GRCm39) |
|
probably benign |
Het |
Vnn3 |
A |
T |
10: 23,741,828 (GRCm39) |
M378L |
probably benign |
Het |
Vps18 |
T |
A |
2: 119,119,538 (GRCm39) |
D6E |
probably benign |
Het |
Xkr5 |
T |
A |
8: 18,989,134 (GRCm39) |
I253F |
probably benign |
Het |
Yeats4 |
A |
T |
10: 117,051,628 (GRCm39) |
C210S |
probably benign |
Het |
Zdhhc20 |
A |
G |
14: 58,076,545 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Rp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Rp1
|
APN |
1 |
4,416,969 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00593:Rp1
|
APN |
1 |
4,415,626 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL00956:Rp1
|
APN |
1 |
4,422,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01070:Rp1
|
APN |
1 |
4,415,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01531:Rp1
|
APN |
1 |
4,419,168 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01668:Rp1
|
APN |
1 |
4,415,941 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01907:Rp1
|
APN |
1 |
4,418,730 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02055:Rp1
|
APN |
1 |
4,422,745 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02071:Rp1
|
APN |
1 |
4,415,533 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02128:Rp1
|
APN |
1 |
4,417,608 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02244:Rp1
|
APN |
1 |
4,419,003 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02381:Rp1
|
APN |
1 |
4,422,613 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02499:Rp1
|
APN |
1 |
4,419,271 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02619:Rp1
|
APN |
1 |
4,418,673 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02832:Rp1
|
APN |
1 |
4,419,936 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02861:Rp1
|
APN |
1 |
4,416,375 (GRCm39) |
nonsense |
probably null |
|
IGL03288:Rp1
|
APN |
1 |
4,419,747 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03290:Rp1
|
APN |
1 |
4,420,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03303:Rp1
|
APN |
1 |
4,415,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Rp1
|
UTSW |
1 |
4,414,851 (GRCm39) |
missense |
probably benign |
0.36 |
R0111:Rp1
|
UTSW |
1 |
4,414,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R0363:Rp1
|
UTSW |
1 |
4,417,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0440:Rp1
|
UTSW |
1 |
4,415,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Rp1
|
UTSW |
1 |
4,416,970 (GRCm39) |
missense |
probably benign |
0.09 |
R0528:Rp1
|
UTSW |
1 |
4,415,088 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0586:Rp1
|
UTSW |
1 |
4,418,060 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0639:Rp1
|
UTSW |
1 |
4,416,721 (GRCm39) |
missense |
probably benign |
0.00 |
R0856:Rp1
|
UTSW |
1 |
4,414,878 (GRCm39) |
missense |
probably benign |
0.05 |
R0908:Rp1
|
UTSW |
1 |
4,414,878 (GRCm39) |
missense |
probably benign |
0.05 |
R0968:Rp1
|
UTSW |
1 |
4,415,575 (GRCm39) |
missense |
probably benign |
0.00 |
R1099:Rp1
|
UTSW |
1 |
4,422,513 (GRCm39) |
missense |
possibly damaging |
0.45 |
R1242:Rp1
|
UTSW |
1 |
4,415,185 (GRCm39) |
missense |
probably benign |
0.03 |
R1301:Rp1
|
UTSW |
1 |
4,416,159 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1327:Rp1
|
UTSW |
1 |
4,418,193 (GRCm39) |
missense |
probably benign |
0.01 |
R1403:Rp1
|
UTSW |
1 |
4,416,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1403:Rp1
|
UTSW |
1 |
4,416,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1406:Rp1
|
UTSW |
1 |
4,422,144 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1406:Rp1
|
UTSW |
1 |
4,422,144 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1440:Rp1
|
UTSW |
1 |
4,417,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Rp1
|
UTSW |
1 |
4,418,760 (GRCm39) |
missense |
probably benign |
0.20 |
R1509:Rp1
|
UTSW |
1 |
4,417,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R1538:Rp1
|
UTSW |
1 |
4,415,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Rp1
|
UTSW |
1 |
4,419,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Rp1
|
UTSW |
1 |
4,420,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Rp1
|
UTSW |
1 |
4,419,312 (GRCm39) |
missense |
probably benign |
0.00 |
R1799:Rp1
|
UTSW |
1 |
4,419,055 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1848:Rp1
|
UTSW |
1 |
4,417,455 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1908:Rp1
|
UTSW |
1 |
4,418,943 (GRCm39) |
missense |
probably damaging |
0.99 |
R1919:Rp1
|
UTSW |
1 |
4,422,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R2087:Rp1
|
UTSW |
1 |
4,418,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Rp1
|
UTSW |
1 |
4,418,362 (GRCm39) |
missense |
probably damaging |
0.96 |
R2278:Rp1
|
UTSW |
1 |
4,418,250 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2287:Rp1
|
UTSW |
1 |
4,416,182 (GRCm39) |
nonsense |
probably null |
|
R2316:Rp1
|
UTSW |
1 |
4,415,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R2346:Rp1
|
UTSW |
1 |
4,418,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R2878:Rp1
|
UTSW |
1 |
4,418,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R3023:Rp1
|
UTSW |
1 |
4,422,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R3025:Rp1
|
UTSW |
1 |
4,422,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R3716:Rp1
|
UTSW |
1 |
4,419,988 (GRCm39) |
missense |
probably benign |
0.38 |
R3814:Rp1
|
UTSW |
1 |
4,419,931 (GRCm39) |
missense |
probably benign |
|
R3929:Rp1
|
UTSW |
1 |
4,422,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4064:Rp1
|
UTSW |
1 |
4,415,623 (GRCm39) |
missense |
probably benign |
0.08 |
R4426:Rp1
|
UTSW |
1 |
4,418,147 (GRCm39) |
missense |
probably benign |
0.13 |
R4557:Rp1
|
UTSW |
1 |
4,414,886 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4764:Rp1
|
UTSW |
1 |
4,416,101 (GRCm39) |
missense |
probably damaging |
0.96 |
R4845:Rp1
|
UTSW |
1 |
4,419,451 (GRCm39) |
missense |
probably benign |
0.02 |
R4850:Rp1
|
UTSW |
1 |
4,418,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Rp1
|
UTSW |
1 |
4,422,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Rp1
|
UTSW |
1 |
4,422,539 (GRCm39) |
missense |
probably damaging |
0.99 |
R5159:Rp1
|
UTSW |
1 |
4,416,426 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5226:Rp1
|
UTSW |
1 |
4,418,256 (GRCm39) |
missense |
probably benign |
0.01 |
R5327:Rp1
|
UTSW |
1 |
4,419,583 (GRCm39) |
splice site |
probably null |
|
R5352:Rp1
|
UTSW |
1 |
4,417,321 (GRCm39) |
missense |
probably benign |
0.00 |
R5504:Rp1
|
UTSW |
1 |
4,420,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R5527:Rp1
|
UTSW |
1 |
4,416,616 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5529:Rp1
|
UTSW |
1 |
4,416,055 (GRCm39) |
missense |
probably benign |
0.42 |
R5569:Rp1
|
UTSW |
1 |
4,415,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R5622:Rp1
|
UTSW |
1 |
4,418,060 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5970:Rp1
|
UTSW |
1 |
4,418,685 (GRCm39) |
missense |
probably benign |
0.05 |
R5992:Rp1
|
UTSW |
1 |
4,218,926 (GRCm39) |
missense |
unknown |
|
R6004:Rp1
|
UTSW |
1 |
4,267,808 (GRCm39) |
missense |
unknown |
|
R6018:Rp1
|
UTSW |
1 |
4,423,059 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6074:Rp1
|
UTSW |
1 |
4,415,602 (GRCm39) |
missense |
probably benign |
0.02 |
R6127:Rp1
|
UTSW |
1 |
4,419,534 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6187:Rp1
|
UTSW |
1 |
4,420,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R6301:Rp1
|
UTSW |
1 |
4,417,477 (GRCm39) |
missense |
probably benign |
0.04 |
R6317:Rp1
|
UTSW |
1 |
4,112,212 (GRCm39) |
missense |
unknown |
|
R6405:Rp1
|
UTSW |
1 |
4,415,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R6445:Rp1
|
UTSW |
1 |
4,296,840 (GRCm39) |
missense |
unknown |
|
R6466:Rp1
|
UTSW |
1 |
4,418,109 (GRCm39) |
missense |
probably benign |
0.01 |
R6501:Rp1
|
UTSW |
1 |
4,381,503 (GRCm39) |
intron |
probably benign |
|
R6547:Rp1
|
UTSW |
1 |
4,240,528 (GRCm39) |
missense |
unknown |
|
R6604:Rp1
|
UTSW |
1 |
4,089,351 (GRCm39) |
missense |
unknown |
|
R6700:Rp1
|
UTSW |
1 |
4,420,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R6706:Rp1
|
UTSW |
1 |
4,212,887 (GRCm39) |
missense |
unknown |
|
R6831:Rp1
|
UTSW |
1 |
4,420,087 (GRCm39) |
splice site |
probably null |
|
R6918:Rp1
|
UTSW |
1 |
4,069,831 (GRCm39) |
missense |
unknown |
|
R6973:Rp1
|
UTSW |
1 |
4,422,217 (GRCm39) |
nonsense |
probably null |
|
R6981:Rp1
|
UTSW |
1 |
4,415,878 (GRCm39) |
missense |
probably benign |
0.06 |
R7009:Rp1
|
UTSW |
1 |
4,112,291 (GRCm39) |
missense |
unknown |
|
R7078:Rp1
|
UTSW |
1 |
4,277,014 (GRCm39) |
missense |
unknown |
|
R7112:Rp1
|
UTSW |
1 |
4,419,241 (GRCm39) |
missense |
probably benign |
0.43 |
R7135:Rp1
|
UTSW |
1 |
4,418,391 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7165:Rp1
|
UTSW |
1 |
4,420,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R7199:Rp1
|
UTSW |
1 |
4,417,513 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7232:Rp1
|
UTSW |
1 |
4,298,824 (GRCm39) |
missense |
unknown |
|
R7367:Rp1
|
UTSW |
1 |
4,418,221 (GRCm39) |
missense |
probably benign |
0.42 |
R7484:Rp1
|
UTSW |
1 |
4,415,704 (GRCm39) |
missense |
probably benign |
0.10 |
R7500:Rp1
|
UTSW |
1 |
4,381,501 (GRCm39) |
missense |
unknown |
|
R7569:Rp1
|
UTSW |
1 |
4,355,063 (GRCm39) |
missense |
unknown |
|
R7642:Rp1
|
UTSW |
1 |
4,218,054 (GRCm39) |
missense |
unknown |
|
R7693:Rp1
|
UTSW |
1 |
4,417,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Rp1
|
UTSW |
1 |
4,240,457 (GRCm39) |
missense |
unknown |
|
R7759:Rp1
|
UTSW |
1 |
4,415,107 (GRCm39) |
missense |
probably benign |
|
R7784:Rp1
|
UTSW |
1 |
4,212,881 (GRCm39) |
missense |
unknown |
|
R7816:Rp1
|
UTSW |
1 |
4,417,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R7866:Rp1
|
UTSW |
1 |
4,417,924 (GRCm39) |
missense |
probably benign |
0.02 |
R8215:Rp1
|
UTSW |
1 |
4,315,318 (GRCm39) |
missense |
unknown |
|
R8281:Rp1
|
UTSW |
1 |
4,418,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R8294:Rp1
|
UTSW |
1 |
4,416,220 (GRCm39) |
missense |
probably benign |
0.09 |
R8309:Rp1
|
UTSW |
1 |
4,417,312 (GRCm39) |
missense |
probably benign |
0.00 |
R8311:Rp1
|
UTSW |
1 |
4,418,572 (GRCm39) |
missense |
probably benign |
0.11 |
R8500:Rp1
|
UTSW |
1 |
4,416,813 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8559:Rp1
|
UTSW |
1 |
4,419,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R8672:Rp1
|
UTSW |
1 |
4,419,007 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8688:Rp1
|
UTSW |
1 |
4,416,628 (GRCm39) |
missense |
probably benign |
0.01 |
R8792:Rp1
|
UTSW |
1 |
4,095,091 (GRCm39) |
missense |
unknown |
|
R8859:Rp1
|
UTSW |
1 |
4,420,183 (GRCm39) |
missense |
probably benign |
0.07 |
R8945:Rp1
|
UTSW |
1 |
4,419,817 (GRCm39) |
missense |
probably benign |
0.42 |
R8959:Rp1
|
UTSW |
1 |
4,419,650 (GRCm39) |
intron |
probably benign |
|
R8979:Rp1
|
UTSW |
1 |
4,218,937 (GRCm39) |
missense |
unknown |
|
R9126:Rp1
|
UTSW |
1 |
4,417,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R9156:Rp1
|
UTSW |
1 |
4,234,161 (GRCm39) |
missense |
unknown |
|
R9160:Rp1
|
UTSW |
1 |
4,416,720 (GRCm39) |
missense |
probably benign |
0.00 |
R9221:Rp1
|
UTSW |
1 |
4,315,266 (GRCm39) |
missense |
unknown |
|
R9263:Rp1
|
UTSW |
1 |
4,419,160 (GRCm39) |
missense |
probably benign |
0.02 |
R9263:Rp1
|
UTSW |
1 |
4,418,675 (GRCm39) |
missense |
probably benign |
0.25 |
R9302:Rp1
|
UTSW |
1 |
4,416,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Rp1
|
UTSW |
1 |
4,418,488 (GRCm39) |
missense |
probably benign |
0.09 |
R9414:Rp1
|
UTSW |
1 |
4,313,841 (GRCm39) |
missense |
unknown |
|
R9474:Rp1
|
UTSW |
1 |
4,162,838 (GRCm39) |
critical splice donor site |
probably null |
|
R9478:Rp1
|
UTSW |
1 |
4,417,545 (GRCm39) |
missense |
probably benign |
0.06 |
R9529:Rp1
|
UTSW |
1 |
4,416,447 (GRCm39) |
missense |
probably benign |
|
R9572:Rp1
|
UTSW |
1 |
4,418,662 (GRCm39) |
missense |
probably benign |
|
R9673:Rp1
|
UTSW |
1 |
4,337,792 (GRCm39) |
missense |
unknown |
|
R9709:Rp1
|
UTSW |
1 |
4,112,255 (GRCm39) |
missense |
unknown |
|
R9716:Rp1
|
UTSW |
1 |
4,212,833 (GRCm39) |
critical splice donor site |
probably null |
|
RF003:Rp1
|
UTSW |
1 |
4,414,917 (GRCm39) |
missense |
probably damaging |
0.99 |
V1662:Rp1
|
UTSW |
1 |
4,419,783 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Rp1
|
UTSW |
1 |
4,417,918 (GRCm39) |
missense |
probably damaging |
0.96 |
|