Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
T |
G |
15: 64,689,488 (GRCm39) |
|
probably null |
Het |
Ank2 |
T |
C |
3: 126,737,886 (GRCm39) |
D2579G |
probably damaging |
Het |
Atp6v1b1 |
G |
C |
6: 83,735,115 (GRCm39) |
G423R |
probably damaging |
Het |
B4galnt3 |
T |
C |
6: 120,191,801 (GRCm39) |
N644S |
probably benign |
Het |
Bhmt1b |
C |
A |
18: 87,775,231 (GRCm39) |
Y251* |
probably null |
Het |
Capsl |
T |
G |
15: 9,465,920 (GRCm39) |
M132R |
probably damaging |
Het |
Cep120 |
A |
G |
18: 53,836,295 (GRCm39) |
Y797H |
probably benign |
Het |
Cimip4 |
T |
C |
15: 78,263,013 (GRCm39) |
T214A |
probably damaging |
Het |
Clec2e |
T |
A |
6: 129,072,061 (GRCm39) |
D106V |
possibly damaging |
Het |
Col6a2 |
C |
T |
10: 76,440,004 (GRCm39) |
V634I |
possibly damaging |
Het |
Dis3 |
T |
C |
14: 99,336,215 (GRCm39) |
E97G |
probably benign |
Het |
Dlec1 |
T |
C |
9: 118,939,281 (GRCm39) |
|
probably null |
Het |
Dock2 |
C |
A |
11: 34,197,789 (GRCm39) |
V1484F |
possibly damaging |
Het |
Ephb2 |
T |
A |
4: 136,388,816 (GRCm39) |
M593L |
probably benign |
Het |
Fcgrt |
T |
C |
7: 44,751,484 (GRCm39) |
T125A |
probably benign |
Het |
Gabbr1 |
T |
C |
17: 37,359,319 (GRCm39) |
I98T |
probably benign |
Het |
Gbp10 |
G |
A |
5: 105,384,015 (GRCm39) |
|
probably benign |
Het |
Gfod1 |
T |
C |
13: 43,354,514 (GRCm39) |
S154G |
possibly damaging |
Het |
Ggt5 |
C |
T |
10: 75,445,160 (GRCm39) |
T389I |
probably damaging |
Het |
Got2 |
A |
G |
8: 96,598,896 (GRCm39) |
F169L |
probably benign |
Het |
Gse1 |
A |
G |
8: 121,215,866 (GRCm39) |
K5E |
possibly damaging |
Het |
Hyal5 |
T |
C |
6: 24,891,437 (GRCm39) |
I417T |
possibly damaging |
Het |
Igkv4-91 |
G |
T |
6: 68,745,607 (GRCm39) |
T97K |
probably damaging |
Het |
Il4i1 |
T |
C |
7: 44,489,608 (GRCm39) |
Y458H |
possibly damaging |
Het |
Impg1 |
A |
T |
9: 80,230,106 (GRCm39) |
C740S |
probably damaging |
Het |
Itgb1 |
C |
G |
8: 129,458,535 (GRCm39) |
T788R |
possibly damaging |
Het |
Lman2l |
A |
G |
1: 36,477,907 (GRCm39) |
V143A |
probably damaging |
Het |
Ltbp4 |
G |
T |
7: 27,029,587 (GRCm39) |
T136K |
unknown |
Het |
Macf1 |
A |
G |
4: 123,366,073 (GRCm39) |
I1331T |
probably benign |
Het |
Mmp11 |
G |
A |
10: 75,762,325 (GRCm39) |
A336V |
probably damaging |
Het |
Myh2 |
A |
T |
11: 67,071,879 (GRCm39) |
I536F |
probably damaging |
Het |
Myh4 |
A |
G |
11: 67,141,618 (GRCm39) |
M826V |
probably benign |
Het |
Naca |
T |
C |
10: 127,875,160 (GRCm39) |
|
probably benign |
Het |
Nr4a2 |
A |
G |
2: 57,002,364 (GRCm39) |
Y30H |
probably damaging |
Het |
Or12j4 |
A |
G |
7: 140,046,758 (GRCm39) |
T215A |
probably benign |
Het |
Or1e35 |
A |
T |
11: 73,797,447 (GRCm39) |
Y290* |
probably null |
Het |
Or2n1d |
T |
A |
17: 38,646,064 (GRCm39) |
N5K |
probably damaging |
Het |
Or4a67 |
T |
A |
2: 88,597,934 (GRCm39) |
I242L |
probably benign |
Het |
Or4f14d |
A |
T |
2: 111,960,445 (GRCm39) |
L237Q |
probably damaging |
Het |
Or4k42 |
A |
T |
2: 111,320,095 (GRCm39) |
M136K |
probably damaging |
Het |
Or4z4 |
A |
G |
19: 12,076,484 (GRCm39) |
V173A |
possibly damaging |
Het |
Or8g22 |
T |
A |
9: 38,958,671 (GRCm39) |
M15L |
possibly damaging |
Het |
Paqr3 |
A |
C |
5: 97,256,128 (GRCm39) |
L82R |
probably damaging |
Het |
Pex6 |
C |
T |
17: 47,031,567 (GRCm39) |
P456S |
probably benign |
Het |
Pih1d2 |
A |
T |
9: 50,532,452 (GRCm39) |
K186I |
possibly damaging |
Het |
Plekhh3 |
A |
G |
11: 101,061,013 (GRCm39) |
|
probably benign |
Het |
Ptpn23 |
C |
A |
9: 110,216,849 (GRCm39) |
|
probably benign |
Het |
Rcor3 |
T |
A |
1: 191,812,142 (GRCm39) |
|
probably benign |
Het |
Rgs11 |
T |
A |
17: 26,429,439 (GRCm39) |
Y403* |
probably null |
Het |
Scn10a |
T |
C |
9: 119,464,649 (GRCm39) |
N984D |
probably benign |
Het |
Snx14 |
C |
T |
9: 88,289,392 (GRCm39) |
A287T |
possibly damaging |
Het |
Stx3 |
T |
C |
19: 11,780,874 (GRCm39) |
D33G |
probably damaging |
Het |
Tacc2 |
A |
G |
7: 130,227,494 (GRCm39) |
K1393R |
probably damaging |
Het |
Tas2r129 |
T |
C |
6: 132,928,455 (GRCm39) |
S131P |
probably benign |
Het |
Tbx15 |
G |
T |
3: 99,220,431 (GRCm39) |
|
probably null |
Het |
Thada |
A |
G |
17: 84,700,795 (GRCm39) |
V1237A |
probably damaging |
Het |
Tnc |
A |
G |
4: 63,888,589 (GRCm39) |
Y1735H |
probably damaging |
Het |
Ttc22 |
A |
G |
4: 106,495,780 (GRCm39) |
K378R |
probably benign |
Het |
Tubg2 |
A |
G |
11: 101,051,635 (GRCm39) |
K287E |
possibly damaging |
Het |
Ugt3a1 |
T |
C |
15: 9,310,762 (GRCm39) |
I348T |
possibly damaging |
Het |
Unc80 |
A |
T |
1: 66,651,409 (GRCm39) |
I1585F |
probably benign |
Het |
Vmn2r104 |
T |
C |
17: 20,261,909 (GRCm39) |
Y407C |
probably damaging |
Het |
Vmn2r108 |
T |
A |
17: 20,692,447 (GRCm39) |
L136F |
probably benign |
Het |
Vmn2r38 |
A |
G |
7: 9,097,611 (GRCm39) |
S161P |
probably damaging |
Het |
Vmn2r90 |
T |
C |
17: 17,953,606 (GRCm39) |
I590T |
probably benign |
Het |
Washc5 |
T |
C |
15: 59,217,248 (GRCm39) |
E323G |
probably damaging |
Het |
Wdhd1 |
C |
T |
14: 47,505,653 (GRCm39) |
G273D |
probably damaging |
Het |
Xpo6 |
G |
T |
7: 125,708,016 (GRCm39) |
Q851K |
probably damaging |
Het |
Zfp386 |
T |
C |
12: 116,023,526 (GRCm39) |
S380P |
probably damaging |
Het |
Zfp536 |
A |
G |
7: 37,173,281 (GRCm39) |
C274R |
unknown |
Het |
Zfp64 |
A |
G |
2: 168,768,088 (GRCm39) |
I508T |
probably benign |
Het |
|
Other mutations in Unc79 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00718:Unc79
|
APN |
12 |
103,135,906 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00835:Unc79
|
APN |
12 |
103,108,149 (GRCm39) |
splice site |
probably benign |
|
IGL00917:Unc79
|
APN |
12 |
103,054,766 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01012:Unc79
|
APN |
12 |
103,078,714 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01121:Unc79
|
APN |
12 |
103,131,890 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01303:Unc79
|
APN |
12 |
103,128,126 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01305:Unc79
|
APN |
12 |
102,968,130 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01315:Unc79
|
APN |
12 |
103,054,780 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01388:Unc79
|
APN |
12 |
103,136,018 (GRCm39) |
splice site |
probably benign |
|
IGL01415:Unc79
|
APN |
12 |
103,074,944 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01447:Unc79
|
APN |
12 |
103,045,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01655:Unc79
|
APN |
12 |
103,134,546 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01662:Unc79
|
APN |
12 |
103,115,279 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01728:Unc79
|
APN |
12 |
103,131,943 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01767:Unc79
|
APN |
12 |
103,108,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02080:Unc79
|
APN |
12 |
102,968,234 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02115:Unc79
|
APN |
12 |
102,964,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02176:Unc79
|
APN |
12 |
102,965,006 (GRCm39) |
splice site |
probably null |
|
IGL02186:Unc79
|
APN |
12 |
102,977,542 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02205:Unc79
|
APN |
12 |
103,045,260 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02337:Unc79
|
APN |
12 |
103,122,705 (GRCm39) |
splice site |
probably benign |
|
IGL02498:Unc79
|
APN |
12 |
103,137,837 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02508:Unc79
|
APN |
12 |
103,078,535 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02508:Unc79
|
APN |
12 |
103,078,277 (GRCm39) |
splice site |
probably benign |
|
IGL02557:Unc79
|
APN |
12 |
103,148,418 (GRCm39) |
splice site |
probably benign |
|
IGL02589:Unc79
|
APN |
12 |
103,139,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02611:Unc79
|
APN |
12 |
103,131,967 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02728:Unc79
|
APN |
12 |
103,088,688 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02827:Unc79
|
APN |
12 |
103,041,105 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03028:Unc79
|
APN |
12 |
103,139,785 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03144:Unc79
|
APN |
12 |
103,008,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03229:Unc79
|
APN |
12 |
103,100,798 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03269:Unc79
|
APN |
12 |
103,054,936 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03325:Unc79
|
APN |
12 |
103,135,869 (GRCm39) |
missense |
probably damaging |
0.98 |
pencil-thin
|
UTSW |
12 |
103,075,040 (GRCm39) |
splice site |
probably null |
|
sweetpea
|
UTSW |
12 |
103,025,777 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Unc79
|
UTSW |
12 |
103,039,009 (GRCm39) |
nonsense |
probably null |
|
ANU22:Unc79
|
UTSW |
12 |
102,968,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R0046:Unc79
|
UTSW |
12 |
103,091,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R0046:Unc79
|
UTSW |
12 |
103,091,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R0067:Unc79
|
UTSW |
12 |
103,025,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R0067:Unc79
|
UTSW |
12 |
103,025,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Unc79
|
UTSW |
12 |
103,100,784 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0110:Unc79
|
UTSW |
12 |
103,045,329 (GRCm39) |
critical splice donor site |
probably null |
|
R0128:Unc79
|
UTSW |
12 |
103,054,693 (GRCm39) |
splice site |
probably benign |
|
R0166:Unc79
|
UTSW |
12 |
103,122,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Unc79
|
UTSW |
12 |
103,058,286 (GRCm39) |
missense |
probably benign |
0.00 |
R0211:Unc79
|
UTSW |
12 |
103,039,051 (GRCm39) |
missense |
probably benign |
0.01 |
R0211:Unc79
|
UTSW |
12 |
103,039,051 (GRCm39) |
missense |
probably benign |
0.01 |
R0218:Unc79
|
UTSW |
12 |
103,075,040 (GRCm39) |
splice site |
probably null |
|
R0244:Unc79
|
UTSW |
12 |
103,079,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0305:Unc79
|
UTSW |
12 |
103,079,459 (GRCm39) |
missense |
probably benign |
0.18 |
R0310:Unc79
|
UTSW |
12 |
103,027,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Unc79
|
UTSW |
12 |
103,137,903 (GRCm39) |
missense |
probably damaging |
0.98 |
R0369:Unc79
|
UTSW |
12 |
103,055,031 (GRCm39) |
critical splice donor site |
probably null |
|
R0450:Unc79
|
UTSW |
12 |
103,045,329 (GRCm39) |
critical splice donor site |
probably null |
|
R0503:Unc79
|
UTSW |
12 |
103,045,127 (GRCm39) |
missense |
probably benign |
0.01 |
R0542:Unc79
|
UTSW |
12 |
103,060,437 (GRCm39) |
splice site |
probably benign |
|
R0845:Unc79
|
UTSW |
12 |
103,139,703 (GRCm39) |
splice site |
probably benign |
|
R0893:Unc79
|
UTSW |
12 |
102,957,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Unc79
|
UTSW |
12 |
103,041,112 (GRCm39) |
missense |
probably benign |
0.03 |
R1148:Unc79
|
UTSW |
12 |
103,078,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Unc79
|
UTSW |
12 |
103,078,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1159:Unc79
|
UTSW |
12 |
103,013,311 (GRCm39) |
splice site |
probably benign |
|
R1191:Unc79
|
UTSW |
12 |
103,013,271 (GRCm39) |
nonsense |
probably null |
|
R1307:Unc79
|
UTSW |
12 |
103,036,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R1368:Unc79
|
UTSW |
12 |
103,122,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1476:Unc79
|
UTSW |
12 |
103,149,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Unc79
|
UTSW |
12 |
103,079,052 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1777:Unc79
|
UTSW |
12 |
103,078,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1796:Unc79
|
UTSW |
12 |
103,109,005 (GRCm39) |
missense |
probably damaging |
0.99 |
R1824:Unc79
|
UTSW |
12 |
103,025,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R1830:Unc79
|
UTSW |
12 |
103,100,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1927:Unc79
|
UTSW |
12 |
103,135,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Unc79
|
UTSW |
12 |
103,041,178 (GRCm39) |
missense |
probably benign |
0.19 |
R1958:Unc79
|
UTSW |
12 |
102,957,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Unc79
|
UTSW |
12 |
102,977,538 (GRCm39) |
nonsense |
probably null |
|
R2019:Unc79
|
UTSW |
12 |
103,137,830 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2290:Unc79
|
UTSW |
12 |
103,112,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2939:Unc79
|
UTSW |
12 |
102,957,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R2962:Unc79
|
UTSW |
12 |
103,061,378 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3176:Unc79
|
UTSW |
12 |
103,079,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R3276:Unc79
|
UTSW |
12 |
103,079,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Unc79
|
UTSW |
12 |
103,041,062 (GRCm39) |
missense |
probably benign |
0.00 |
R3684:Unc79
|
UTSW |
12 |
103,041,062 (GRCm39) |
missense |
probably benign |
0.00 |
R3686:Unc79
|
UTSW |
12 |
103,054,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R3760:Unc79
|
UTSW |
12 |
103,058,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R4031:Unc79
|
UTSW |
12 |
103,039,018 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4039:Unc79
|
UTSW |
12 |
103,041,208 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4110:Unc79
|
UTSW |
12 |
103,025,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4113:Unc79
|
UTSW |
12 |
103,025,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4159:Unc79
|
UTSW |
12 |
103,036,512 (GRCm39) |
intron |
probably benign |
|
R4273:Unc79
|
UTSW |
12 |
103,088,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R4292:Unc79
|
UTSW |
12 |
103,149,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R4334:Unc79
|
UTSW |
12 |
103,045,233 (GRCm39) |
missense |
probably benign |
|
R4513:Unc79
|
UTSW |
12 |
102,988,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R4562:Unc79
|
UTSW |
12 |
102,957,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Unc79
|
UTSW |
12 |
102,968,062 (GRCm39) |
splice site |
probably benign |
|
R4645:Unc79
|
UTSW |
12 |
103,079,081 (GRCm39) |
missense |
probably benign |
|
R4758:Unc79
|
UTSW |
12 |
103,128,080 (GRCm39) |
nonsense |
probably null |
|
R4787:Unc79
|
UTSW |
12 |
103,013,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R4852:Unc79
|
UTSW |
12 |
103,139,725 (GRCm39) |
missense |
probably damaging |
0.98 |
R4883:Unc79
|
UTSW |
12 |
103,060,592 (GRCm39) |
missense |
probably damaging |
0.99 |
R4898:Unc79
|
UTSW |
12 |
103,128,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R4979:Unc79
|
UTSW |
12 |
103,078,691 (GRCm39) |
missense |
probably benign |
|
R5044:Unc79
|
UTSW |
12 |
103,078,962 (GRCm39) |
missense |
probably benign |
0.32 |
R5053:Unc79
|
UTSW |
12 |
103,071,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5061:Unc79
|
UTSW |
12 |
103,134,700 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5075:Unc79
|
UTSW |
12 |
103,041,213 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5101:Unc79
|
UTSW |
12 |
103,078,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R5236:Unc79
|
UTSW |
12 |
103,060,654 (GRCm39) |
critical splice donor site |
probably null |
|
R5240:Unc79
|
UTSW |
12 |
103,037,010 (GRCm39) |
missense |
probably damaging |
0.99 |
R5383:Unc79
|
UTSW |
12 |
103,070,886 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5461:Unc79
|
UTSW |
12 |
103,078,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R5535:Unc79
|
UTSW |
12 |
103,135,962 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5609:Unc79
|
UTSW |
12 |
103,094,527 (GRCm39) |
missense |
probably benign |
|
R5639:Unc79
|
UTSW |
12 |
103,137,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R5704:Unc79
|
UTSW |
12 |
102,968,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R5923:Unc79
|
UTSW |
12 |
103,078,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R5925:Unc79
|
UTSW |
12 |
103,091,989 (GRCm39) |
splice site |
probably null |
|
R5975:Unc79
|
UTSW |
12 |
103,091,885 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6047:Unc79
|
UTSW |
12 |
103,027,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Unc79
|
UTSW |
12 |
103,149,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R6292:Unc79
|
UTSW |
12 |
103,108,991 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6313:Unc79
|
UTSW |
12 |
103,078,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R6391:Unc79
|
UTSW |
12 |
102,987,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R6405:Unc79
|
UTSW |
12 |
103,134,595 (GRCm39) |
missense |
probably damaging |
0.97 |
R6416:Unc79
|
UTSW |
12 |
103,097,905 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6467:Unc79
|
UTSW |
12 |
103,139,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Unc79
|
UTSW |
12 |
103,027,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R6614:Unc79
|
UTSW |
12 |
102,957,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Unc79
|
UTSW |
12 |
103,045,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Unc79
|
UTSW |
12 |
103,045,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R6700:Unc79
|
UTSW |
12 |
103,091,962 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6724:Unc79
|
UTSW |
12 |
103,071,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R6819:Unc79
|
UTSW |
12 |
103,108,267 (GRCm39) |
missense |
probably benign |
0.12 |
R6869:Unc79
|
UTSW |
12 |
103,079,331 (GRCm39) |
missense |
probably benign |
0.33 |
R6879:Unc79
|
UTSW |
12 |
103,115,046 (GRCm39) |
splice site |
probably null |
|
R6942:Unc79
|
UTSW |
12 |
103,088,704 (GRCm39) |
critical splice donor site |
probably null |
|
R6961:Unc79
|
UTSW |
12 |
103,079,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Unc79
|
UTSW |
12 |
102,964,699 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6980:Unc79
|
UTSW |
12 |
103,025,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7124:Unc79
|
UTSW |
12 |
103,027,652 (GRCm39) |
missense |
probably damaging |
0.99 |
R7144:Unc79
|
UTSW |
12 |
103,108,885 (GRCm39) |
missense |
probably benign |
0.06 |
R7197:Unc79
|
UTSW |
12 |
103,078,765 (GRCm39) |
missense |
probably benign |
|
R7209:Unc79
|
UTSW |
12 |
103,091,883 (GRCm39) |
missense |
probably benign |
|
R7232:Unc79
|
UTSW |
12 |
103,100,734 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7304:Unc79
|
UTSW |
12 |
103,029,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7354:Unc79
|
UTSW |
12 |
103,108,961 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7384:Unc79
|
UTSW |
12 |
103,137,837 (GRCm39) |
missense |
probably benign |
0.11 |
R7400:Unc79
|
UTSW |
12 |
103,070,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R7417:Unc79
|
UTSW |
12 |
103,055,017 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7470:Unc79
|
UTSW |
12 |
103,061,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Unc79
|
UTSW |
12 |
103,058,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R8037:Unc79
|
UTSW |
12 |
103,016,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R8041:Unc79
|
UTSW |
12 |
103,054,726 (GRCm39) |
missense |
probably benign |
0.06 |
R8146:Unc79
|
UTSW |
12 |
103,036,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R8276:Unc79
|
UTSW |
12 |
102,968,122 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8427:Unc79
|
UTSW |
12 |
103,045,297 (GRCm39) |
missense |
probably benign |
0.24 |
R8501:Unc79
|
UTSW |
12 |
103,058,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R8510:Unc79
|
UTSW |
12 |
103,070,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Unc79
|
UTSW |
12 |
103,013,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Unc79
|
UTSW |
12 |
103,049,855 (GRCm39) |
missense |
probably benign |
0.13 |
R8795:Unc79
|
UTSW |
12 |
103,074,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R9017:Unc79
|
UTSW |
12 |
103,074,874 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9121:Unc79
|
UTSW |
12 |
102,968,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R9196:Unc79
|
UTSW |
12 |
103,078,613 (GRCm39) |
missense |
probably benign |
|
R9443:Unc79
|
UTSW |
12 |
103,037,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R9548:Unc79
|
UTSW |
12 |
102,977,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R9600:Unc79
|
UTSW |
12 |
103,135,972 (GRCm39) |
missense |
probably benign |
0.07 |
R9767:Unc79
|
UTSW |
12 |
103,079,234 (GRCm39) |
missense |
probably benign |
|
R9787:Unc79
|
UTSW |
12 |
103,112,620 (GRCm39) |
missense |
probably benign |
0.00 |
RF010:Unc79
|
UTSW |
12 |
103,079,046 (GRCm39) |
missense |
probably benign |
0.17 |
X0017:Unc79
|
UTSW |
12 |
103,074,520 (GRCm39) |
missense |
probably damaging |
0.99 |
X0028:Unc79
|
UTSW |
12 |
102,957,662 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Unc79
|
UTSW |
12 |
102,987,271 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Unc79
|
UTSW |
12 |
103,108,312 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Unc79
|
UTSW |
12 |
103,054,937 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Unc79
|
UTSW |
12 |
103,131,948 (GRCm39) |
missense |
probably benign |
|
|