Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
T |
A |
11: 58,771,020 (GRCm39) |
H167Q |
probably benign |
Het |
Adamts20 |
T |
C |
15: 94,277,827 (GRCm39) |
T212A |
probably benign |
Het |
Ap3b1 |
C |
A |
13: 94,554,607 (GRCm39) |
L248I |
probably damaging |
Het |
Atl1 |
T |
G |
12: 70,005,973 (GRCm39) |
D426E |
probably benign |
Het |
Cage1 |
T |
A |
13: 38,207,078 (GRCm39) |
I256F |
probably damaging |
Het |
Calcr |
A |
T |
6: 3,708,484 (GRCm39) |
|
probably null |
Het |
Canx |
T |
C |
11: 50,195,265 (GRCm39) |
T268A |
probably benign |
Het |
Chd7 |
A |
T |
4: 8,866,353 (GRCm39) |
M842L |
possibly damaging |
Het |
Clca4a |
T |
C |
3: 144,658,609 (GRCm39) |
T787A |
probably benign |
Het |
Clstn3 |
T |
C |
6: 124,433,939 (GRCm39) |
Y407C |
probably damaging |
Het |
Copa |
C |
A |
1: 171,929,791 (GRCm39) |
T286N |
probably damaging |
Het |
Cyb5a |
G |
A |
18: 84,889,718 (GRCm39) |
R49Q |
possibly damaging |
Het |
Def6 |
A |
G |
17: 28,438,950 (GRCm39) |
K219E |
probably damaging |
Het |
Eif4g1 |
G |
T |
16: 20,497,593 (GRCm39) |
|
probably benign |
Het |
Eif5 |
A |
T |
12: 111,508,183 (GRCm39) |
K161N |
probably benign |
Het |
Fras1 |
C |
A |
5: 96,790,479 (GRCm39) |
T951K |
probably damaging |
Het |
Gen1 |
A |
T |
12: 11,292,363 (GRCm39) |
N475K |
possibly damaging |
Het |
Gm14569 |
T |
C |
X: 35,697,146 (GRCm39) |
Y521C |
probably benign |
Het |
Gm6124 |
T |
A |
7: 38,870,529 (GRCm39) |
|
noncoding transcript |
Het |
Gpt2 |
A |
T |
8: 86,252,188 (GRCm39) |
D501V |
probably benign |
Het |
Gstm2 |
T |
C |
3: 107,893,370 (GRCm39) |
K31R |
probably benign |
Het |
Homer3 |
G |
A |
8: 70,742,793 (GRCm39) |
|
probably null |
Het |
Itga1 |
T |
A |
13: 115,138,102 (GRCm39) |
M428L |
probably benign |
Het |
Kalrn |
C |
T |
16: 33,810,180 (GRCm39) |
D2525N |
possibly damaging |
Het |
Kcnn4 |
T |
C |
7: 24,076,867 (GRCm39) |
W139R |
probably benign |
Het |
Kdm7a |
T |
A |
6: 39,143,602 (GRCm39) |
R380W |
probably null |
Het |
Khdrbs1 |
T |
G |
4: 129,635,889 (GRCm39) |
D22A |
possibly damaging |
Het |
Liph |
A |
T |
16: 21,795,000 (GRCm39) |
I204N |
probably damaging |
Het |
Loxhd1 |
A |
G |
18: 77,529,456 (GRCm39) |
E2033G |
possibly damaging |
Het |
M6pr |
C |
T |
6: 122,291,982 (GRCm39) |
|
probably benign |
Het |
Mrm1 |
A |
G |
11: 84,709,915 (GRCm39) |
I95T |
probably damaging |
Het |
Mroh2a |
G |
T |
1: 88,182,657 (GRCm39) |
R1195L |
possibly damaging |
Het |
Mug1 |
C |
A |
6: 121,856,311 (GRCm39) |
F1030L |
probably damaging |
Het |
Naca |
C |
T |
10: 127,879,341 (GRCm39) |
|
probably benign |
Het |
Nob1 |
A |
T |
8: 108,145,120 (GRCm39) |
|
probably benign |
Het |
Nutm1 |
A |
C |
2: 112,080,154 (GRCm39) |
I587R |
probably damaging |
Het |
Or1e26 |
A |
G |
11: 73,480,081 (GRCm39) |
V161A |
probably benign |
Het |
Pcdhb2 |
A |
G |
18: 37,428,455 (GRCm39) |
K143E |
probably benign |
Het |
Piwil2 |
A |
T |
14: 70,646,365 (GRCm39) |
D390E |
probably benign |
Het |
Pkhd1 |
A |
G |
1: 20,309,635 (GRCm39) |
L2771P |
probably damaging |
Het |
Pla2g1b |
T |
A |
5: 115,608,947 (GRCm39) |
Y47* |
probably null |
Het |
Plekhn1 |
T |
C |
4: 156,309,813 (GRCm39) |
T135A |
probably damaging |
Het |
Pola1 |
T |
C |
X: 92,605,029 (GRCm39) |
Y968C |
probably damaging |
Het |
Ppp1r26 |
C |
A |
2: 28,341,618 (GRCm39) |
T416K |
probably benign |
Het |
Psmd1 |
A |
G |
1: 86,003,673 (GRCm39) |
I153V |
possibly damaging |
Het |
Rcan2 |
A |
G |
17: 44,264,361 (GRCm39) |
D7G |
probably benign |
Het |
Rexo5 |
T |
C |
7: 119,433,599 (GRCm39) |
I326T |
possibly damaging |
Het |
Rps6kc1 |
A |
G |
1: 190,530,802 (GRCm39) |
|
probably benign |
Het |
Shc1 |
T |
C |
3: 89,333,985 (GRCm39) |
S273P |
probably benign |
Het |
Slc9b2 |
T |
C |
3: 135,042,305 (GRCm39) |
V528A |
probably benign |
Het |
Tas2r118 |
T |
C |
6: 23,969,293 (GRCm39) |
K256R |
probably benign |
Het |
Tma16 |
C |
T |
8: 66,936,823 (GRCm39) |
|
probably null |
Het |
Tnfaip2 |
T |
C |
12: 111,416,285 (GRCm39) |
F516L |
probably benign |
Het |
Ugt1a1 |
CAGAGAGAGAGAGA |
CAGAGAGAGAGA |
1: 88,139,706 (GRCm39) |
|
probably benign |
Het |
Ugt1a10 |
C |
T |
1: 88,142,845 (GRCm39) |
P113L |
probably damaging |
Het |
Wdr35 |
A |
G |
12: 9,039,981 (GRCm39) |
D362G |
probably damaging |
Het |
Wwp2 |
T |
C |
8: 108,184,610 (GRCm39) |
V106A |
probably benign |
Het |
Zfp40 |
T |
A |
17: 23,395,693 (GRCm39) |
H230L |
possibly damaging |
Het |
Zkscan17 |
T |
A |
11: 59,393,848 (GRCm39) |
M1L |
possibly damaging |
Het |
|
Other mutations in Pcnt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01075:Pcnt
|
APN |
10 |
76,258,738 (GRCm39) |
nonsense |
probably null |
|
IGL01307:Pcnt
|
APN |
10 |
76,247,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01549:Pcnt
|
APN |
10 |
76,203,320 (GRCm39) |
splice site |
probably null |
|
IGL01576:Pcnt
|
APN |
10 |
76,204,656 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01611:Pcnt
|
APN |
10 |
76,272,258 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01630:Pcnt
|
APN |
10 |
76,256,080 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01647:Pcnt
|
APN |
10 |
76,205,835 (GRCm39) |
nonsense |
probably null |
|
IGL01689:Pcnt
|
APN |
10 |
76,247,487 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01690:Pcnt
|
APN |
10 |
76,228,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01723:Pcnt
|
APN |
10 |
76,254,333 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01920:Pcnt
|
APN |
10 |
76,240,362 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01958:Pcnt
|
APN |
10 |
76,269,513 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02210:Pcnt
|
APN |
10 |
76,225,053 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02225:Pcnt
|
APN |
10 |
76,225,308 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02228:Pcnt
|
APN |
10 |
76,225,308 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02237:Pcnt
|
APN |
10 |
76,188,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02279:Pcnt
|
APN |
10 |
76,239,599 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Pcnt
|
APN |
10 |
76,278,393 (GRCm39) |
splice site |
probably benign |
|
IGL02355:Pcnt
|
APN |
10 |
76,210,996 (GRCm39) |
nonsense |
probably null |
|
IGL02362:Pcnt
|
APN |
10 |
76,210,996 (GRCm39) |
nonsense |
probably null |
|
IGL02428:Pcnt
|
APN |
10 |
76,265,090 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02536:Pcnt
|
APN |
10 |
76,216,063 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02715:Pcnt
|
APN |
10 |
76,204,556 (GRCm39) |
splice site |
probably benign |
|
IGL02800:Pcnt
|
APN |
10 |
76,248,417 (GRCm39) |
nonsense |
probably null |
|
IGL03395:Pcnt
|
APN |
10 |
76,272,325 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02799:Pcnt
|
UTSW |
10 |
76,248,417 (GRCm39) |
nonsense |
probably null |
|
PIT4520001:Pcnt
|
UTSW |
10 |
76,256,069 (GRCm39) |
missense |
probably damaging |
0.99 |
R0049:Pcnt
|
UTSW |
10 |
76,205,655 (GRCm39) |
unclassified |
probably benign |
|
R0049:Pcnt
|
UTSW |
10 |
76,205,655 (GRCm39) |
unclassified |
probably benign |
|
R0109:Pcnt
|
UTSW |
10 |
76,225,030 (GRCm39) |
missense |
probably benign |
0.00 |
R0117:Pcnt
|
UTSW |
10 |
76,244,561 (GRCm39) |
nonsense |
probably null |
|
R0254:Pcnt
|
UTSW |
10 |
76,228,414 (GRCm39) |
missense |
probably benign |
0.10 |
R0392:Pcnt
|
UTSW |
10 |
76,220,660 (GRCm39) |
missense |
probably benign |
|
R0511:Pcnt
|
UTSW |
10 |
76,240,429 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0570:Pcnt
|
UTSW |
10 |
76,247,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Pcnt
|
UTSW |
10 |
76,256,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Pcnt
|
UTSW |
10 |
76,240,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0707:Pcnt
|
UTSW |
10 |
76,256,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R0749:Pcnt
|
UTSW |
10 |
76,217,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0969:Pcnt
|
UTSW |
10 |
76,263,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1174:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1175:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1512:Pcnt
|
UTSW |
10 |
76,240,496 (GRCm39) |
splice site |
probably null |
|
R1542:Pcnt
|
UTSW |
10 |
76,237,220 (GRCm39) |
missense |
probably benign |
0.02 |
R1542:Pcnt
|
UTSW |
10 |
76,225,221 (GRCm39) |
missense |
probably benign |
0.08 |
R1558:Pcnt
|
UTSW |
10 |
76,258,756 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1562:Pcnt
|
UTSW |
10 |
76,203,164 (GRCm39) |
missense |
probably benign |
0.02 |
R1762:Pcnt
|
UTSW |
10 |
76,190,971 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1779:Pcnt
|
UTSW |
10 |
76,244,630 (GRCm39) |
missense |
probably damaging |
0.99 |
R1869:Pcnt
|
UTSW |
10 |
76,215,740 (GRCm39) |
missense |
probably null |
0.94 |
R1911:Pcnt
|
UTSW |
10 |
76,204,650 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1985:Pcnt
|
UTSW |
10 |
76,216,171 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1995:Pcnt
|
UTSW |
10 |
76,228,633 (GRCm39) |
nonsense |
probably null |
|
R2073:Pcnt
|
UTSW |
10 |
76,216,214 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2111:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R2112:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R2309:Pcnt
|
UTSW |
10 |
76,278,460 (GRCm39) |
start gained |
probably benign |
|
R2902:Pcnt
|
UTSW |
10 |
76,211,064 (GRCm39) |
missense |
probably damaging |
0.98 |
R3623:Pcnt
|
UTSW |
10 |
76,269,584 (GRCm39) |
missense |
probably benign |
0.23 |
R4088:Pcnt
|
UTSW |
10 |
76,263,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R4300:Pcnt
|
UTSW |
10 |
76,203,225 (GRCm39) |
missense |
probably benign |
0.40 |
R4407:Pcnt
|
UTSW |
10 |
76,210,704 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4483:Pcnt
|
UTSW |
10 |
76,237,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Pcnt
|
UTSW |
10 |
76,190,047 (GRCm39) |
missense |
probably benign |
0.01 |
R4734:Pcnt
|
UTSW |
10 |
76,273,040 (GRCm39) |
missense |
probably benign |
0.25 |
R4747:Pcnt
|
UTSW |
10 |
76,272,299 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4782:Pcnt
|
UTSW |
10 |
76,245,411 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4795:Pcnt
|
UTSW |
10 |
76,205,858 (GRCm39) |
missense |
probably benign |
0.21 |
R4831:Pcnt
|
UTSW |
10 |
76,248,335 (GRCm39) |
missense |
probably damaging |
0.96 |
R4873:Pcnt
|
UTSW |
10 |
76,205,688 (GRCm39) |
missense |
probably benign |
0.03 |
R4875:Pcnt
|
UTSW |
10 |
76,205,688 (GRCm39) |
missense |
probably benign |
0.03 |
R4946:Pcnt
|
UTSW |
10 |
76,192,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Pcnt
|
UTSW |
10 |
76,190,911 (GRCm39) |
missense |
probably benign |
0.00 |
R5033:Pcnt
|
UTSW |
10 |
76,235,779 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5106:Pcnt
|
UTSW |
10 |
76,237,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R5118:Pcnt
|
UTSW |
10 |
76,248,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R5167:Pcnt
|
UTSW |
10 |
76,256,258 (GRCm39) |
missense |
probably damaging |
0.97 |
R5199:Pcnt
|
UTSW |
10 |
76,254,378 (GRCm39) |
missense |
probably benign |
0.09 |
R5223:Pcnt
|
UTSW |
10 |
76,216,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R5241:Pcnt
|
UTSW |
10 |
76,269,451 (GRCm39) |
missense |
probably benign |
0.26 |
R5308:Pcnt
|
UTSW |
10 |
76,192,159 (GRCm39) |
nonsense |
probably null |
|
R5328:Pcnt
|
UTSW |
10 |
76,247,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R5454:Pcnt
|
UTSW |
10 |
76,225,381 (GRCm39) |
splice site |
probably null |
|
R5543:Pcnt
|
UTSW |
10 |
76,247,886 (GRCm39) |
missense |
probably benign |
0.01 |
R5588:Pcnt
|
UTSW |
10 |
76,278,445 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5647:Pcnt
|
UTSW |
10 |
76,221,675 (GRCm39) |
missense |
probably benign |
0.17 |
R5668:Pcnt
|
UTSW |
10 |
76,245,334 (GRCm39) |
missense |
probably benign |
0.16 |
R5712:Pcnt
|
UTSW |
10 |
76,265,105 (GRCm39) |
missense |
probably damaging |
0.96 |
R5714:Pcnt
|
UTSW |
10 |
76,256,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Pcnt
|
UTSW |
10 |
76,228,590 (GRCm39) |
missense |
probably benign |
0.00 |
R5946:Pcnt
|
UTSW |
10 |
76,217,897 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5955:Pcnt
|
UTSW |
10 |
76,247,456 (GRCm39) |
missense |
possibly damaging |
0.45 |
R6024:Pcnt
|
UTSW |
10 |
76,255,871 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6267:Pcnt
|
UTSW |
10 |
76,221,632 (GRCm39) |
missense |
probably benign |
0.02 |
R6485:Pcnt
|
UTSW |
10 |
76,225,164 (GRCm39) |
nonsense |
probably null |
|
R6605:Pcnt
|
UTSW |
10 |
76,265,032 (GRCm39) |
critical splice donor site |
probably null |
|
R6877:Pcnt
|
UTSW |
10 |
76,269,851 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6882:Pcnt
|
UTSW |
10 |
76,263,662 (GRCm39) |
missense |
probably benign |
0.00 |
R6919:Pcnt
|
UTSW |
10 |
76,221,632 (GRCm39) |
missense |
probably benign |
0.02 |
R7025:Pcnt
|
UTSW |
10 |
76,239,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Pcnt
|
UTSW |
10 |
76,220,673 (GRCm39) |
missense |
probably benign |
|
R7109:Pcnt
|
UTSW |
10 |
76,205,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Pcnt
|
UTSW |
10 |
76,263,761 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7143:Pcnt
|
UTSW |
10 |
76,224,894 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7152:Pcnt
|
UTSW |
10 |
76,247,194 (GRCm39) |
splice site |
probably null |
|
R7213:Pcnt
|
UTSW |
10 |
76,244,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7368:Pcnt
|
UTSW |
10 |
76,235,835 (GRCm39) |
missense |
probably benign |
|
R7453:Pcnt
|
UTSW |
10 |
76,225,284 (GRCm39) |
missense |
probably benign |
|
R7486:Pcnt
|
UTSW |
10 |
76,254,271 (GRCm39) |
missense |
probably benign |
|
R7486:Pcnt
|
UTSW |
10 |
76,254,270 (GRCm39) |
missense |
probably benign |
0.03 |
R7538:Pcnt
|
UTSW |
10 |
76,235,773 (GRCm39) |
missense |
probably benign |
|
R7575:Pcnt
|
UTSW |
10 |
76,225,086 (GRCm39) |
missense |
probably benign |
0.32 |
R7662:Pcnt
|
UTSW |
10 |
76,223,356 (GRCm39) |
missense |
probably benign |
0.27 |
R7685:Pcnt
|
UTSW |
10 |
76,258,642 (GRCm39) |
missense |
probably benign |
0.14 |
R7764:Pcnt
|
UTSW |
10 |
76,190,082 (GRCm39) |
missense |
probably benign |
0.33 |
R7802:Pcnt
|
UTSW |
10 |
76,211,137 (GRCm39) |
splice site |
probably null |
|
R8432:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8439:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8493:Pcnt
|
UTSW |
10 |
76,239,457 (GRCm39) |
critical splice donor site |
probably null |
|
R8530:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8535:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8830:Pcnt
|
UTSW |
10 |
76,218,008 (GRCm39) |
missense |
probably benign |
0.03 |
R8878:Pcnt
|
UTSW |
10 |
76,244,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Pcnt
|
UTSW |
10 |
76,223,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R8988:Pcnt
|
UTSW |
10 |
76,245,407 (GRCm39) |
nonsense |
probably null |
|
R9084:Pcnt
|
UTSW |
10 |
76,235,826 (GRCm39) |
missense |
probably benign |
0.09 |
R9169:Pcnt
|
UTSW |
10 |
76,221,572 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9372:Pcnt
|
UTSW |
10 |
76,258,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R9411:Pcnt
|
UTSW |
10 |
76,258,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R9448:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R9459:Pcnt
|
UTSW |
10 |
76,228,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Pcnt
|
UTSW |
10 |
76,217,963 (GRCm39) |
missense |
probably benign |
0.00 |
R9503:Pcnt
|
UTSW |
10 |
76,263,882 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9561:Pcnt
|
UTSW |
10 |
76,217,128 (GRCm39) |
nonsense |
probably null |
|
R9618:Pcnt
|
UTSW |
10 |
76,188,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R9648:Pcnt
|
UTSW |
10 |
76,190,089 (GRCm39) |
missense |
probably benign |
0.32 |
R9733:Pcnt
|
UTSW |
10 |
76,237,314 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Pcnt
|
UTSW |
10 |
76,217,991 (GRCm39) |
nonsense |
probably null |
|
Z1177:Pcnt
|
UTSW |
10 |
76,235,802 (GRCm39) |
missense |
probably benign |
0.00 |
|