Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
C |
T |
8: 25,164,070 (GRCm39) |
G38R |
probably benign |
Het |
Ap2m1 |
T |
C |
16: 20,359,849 (GRCm39) |
M183T |
probably damaging |
Het |
Apob |
A |
T |
12: 8,038,678 (GRCm39) |
I364F |
probably damaging |
Het |
Arl6 |
A |
T |
16: 59,442,784 (GRCm39) |
|
probably benign |
Het |
Cand2 |
A |
G |
6: 115,751,614 (GRCm39) |
M15V |
possibly damaging |
Het |
Cbl |
A |
G |
9: 44,112,302 (GRCm39) |
F131S |
probably damaging |
Het |
Ccdc74a |
A |
G |
16: 17,468,340 (GRCm39) |
S321G |
probably benign |
Het |
Cdc14b |
T |
C |
13: 64,358,006 (GRCm39) |
|
probably benign |
Het |
Cep152 |
T |
C |
2: 125,418,789 (GRCm39) |
|
probably benign |
Het |
Cep290 |
A |
G |
10: 100,344,620 (GRCm39) |
E479G |
probably benign |
Het |
Chrm2 |
T |
G |
6: 36,501,046 (GRCm39) |
I301R |
probably benign |
Het |
Clec2e |
A |
G |
6: 129,070,431 (GRCm39) |
W197R |
probably damaging |
Het |
Cnot10 |
G |
T |
9: 114,458,218 (GRCm39) |
S96* |
probably null |
Het |
Col19a1 |
A |
G |
1: 24,328,736 (GRCm39) |
|
probably benign |
Het |
Csmd2 |
T |
C |
4: 128,027,466 (GRCm39) |
|
probably benign |
Het |
Cthrc1 |
A |
T |
15: 38,950,159 (GRCm39) |
*172L |
probably null |
Het |
Cul9 |
A |
T |
17: 46,839,515 (GRCm39) |
I821N |
probably benign |
Het |
Daam1 |
G |
C |
12: 72,022,078 (GRCm39) |
|
probably benign |
Het |
Dhx58 |
A |
T |
11: 100,590,090 (GRCm39) |
I398N |
probably damaging |
Het |
Dip2b |
T |
A |
15: 100,091,794 (GRCm39) |
H844Q |
probably damaging |
Het |
Dmac2 |
A |
G |
7: 25,320,454 (GRCm39) |
D50G |
probably damaging |
Het |
Dmxl1 |
C |
A |
18: 50,012,429 (GRCm39) |
Q1529K |
probably benign |
Het |
Dtna |
C |
T |
18: 23,730,558 (GRCm39) |
P315L |
probably damaging |
Het |
Ep300 |
T |
C |
15: 81,524,317 (GRCm39) |
S1382P |
unknown |
Het |
Fat2 |
A |
T |
11: 55,201,603 (GRCm39) |
N490K |
probably damaging |
Het |
Flg2 |
T |
A |
3: 93,107,662 (GRCm39) |
|
probably benign |
Het |
Gpatch1 |
T |
C |
7: 34,980,806 (GRCm39) |
|
probably benign |
Het |
Grin2a |
C |
A |
16: 9,397,449 (GRCm39) |
K879N |
possibly damaging |
Het |
Hacd3 |
A |
C |
9: 64,908,304 (GRCm39) |
I164S |
possibly damaging |
Het |
Hinfp |
A |
C |
9: 44,210,245 (GRCm39) |
C197G |
probably damaging |
Het |
Hsd17b12 |
T |
C |
2: 93,945,335 (GRCm39) |
|
probably benign |
Het |
Hsd3b1 |
A |
T |
3: 98,760,355 (GRCm39) |
L212Q |
probably damaging |
Het |
Ifrd1 |
C |
T |
12: 40,264,093 (GRCm39) |
|
probably null |
Het |
Igf2bp2 |
A |
G |
16: 21,900,551 (GRCm39) |
F129L |
possibly damaging |
Het |
Kirrel3 |
T |
A |
9: 34,931,459 (GRCm39) |
I409N |
probably damaging |
Het |
Klhdc10 |
T |
C |
6: 30,447,411 (GRCm39) |
I204T |
probably damaging |
Het |
Kpna6 |
A |
T |
4: 129,551,597 (GRCm39) |
S65R |
possibly damaging |
Het |
Lama3 |
A |
T |
18: 12,540,620 (GRCm39) |
D308V |
probably benign |
Het |
Larp4b |
T |
A |
13: 9,208,143 (GRCm39) |
|
probably null |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Lyzl1 |
A |
T |
18: 4,169,175 (GRCm39) |
T11S |
probably benign |
Het |
Man1c1 |
A |
G |
4: 134,305,626 (GRCm39) |
L366P |
probably damaging |
Het |
Mef2a |
A |
G |
7: 66,901,472 (GRCm39) |
M100T |
probably damaging |
Het |
Mettl13 |
G |
A |
1: 162,366,458 (GRCm39) |
H474Y |
possibly damaging |
Het |
Minar2 |
T |
A |
18: 59,208,760 (GRCm39) |
V136E |
probably damaging |
Het |
Mmp3 |
A |
G |
9: 7,451,320 (GRCm39) |
D352G |
probably benign |
Het |
Mns1 |
T |
C |
9: 72,360,086 (GRCm39) |
I412T |
probably damaging |
Het |
Mon2 |
T |
C |
10: 122,842,926 (GRCm39) |
D1501G |
probably null |
Het |
Mylk |
G |
T |
16: 34,695,990 (GRCm39) |
G242W |
probably damaging |
Het |
Nav1 |
T |
C |
1: 135,377,704 (GRCm39) |
D1715G |
possibly damaging |
Het |
Nckap1l |
T |
C |
15: 103,362,310 (GRCm39) |
S2P |
probably damaging |
Het |
Nek3 |
A |
T |
8: 22,618,745 (GRCm39) |
|
probably benign |
Het |
Nfrkb |
A |
G |
9: 31,300,193 (GRCm39) |
|
probably benign |
Het |
Nlrp4d |
T |
C |
7: 10,122,705 (GRCm39) |
D53G |
probably benign |
Het |
Nol8 |
T |
C |
13: 49,815,628 (GRCm39) |
S561P |
probably damaging |
Het |
Nuf2 |
A |
C |
1: 169,352,866 (GRCm39) |
|
probably benign |
Het |
Odad3 |
T |
A |
9: 21,903,004 (GRCm39) |
H442L |
probably benign |
Het |
Ofcc1 |
T |
A |
13: 40,168,789 (GRCm39) |
D866V |
possibly damaging |
Het |
Optn |
A |
G |
2: 5,051,006 (GRCm39) |
L125P |
probably benign |
Het |
Or5k3 |
A |
G |
16: 58,969,662 (GRCm39) |
I150V |
probably benign |
Het |
Otoa |
T |
A |
7: 120,730,564 (GRCm39) |
F588Y |
probably benign |
Het |
Pappa |
T |
A |
4: 65,269,850 (GRCm39) |
|
probably null |
Het |
Pde5a |
T |
G |
3: 122,629,232 (GRCm39) |
C635W |
probably damaging |
Het |
Pdgfb |
A |
T |
15: 79,887,620 (GRCm39) |
|
probably null |
Het |
Pih1d2 |
T |
A |
9: 50,532,346 (GRCm39) |
C135S |
probably damaging |
Het |
Plcg1 |
G |
T |
2: 160,594,286 (GRCm39) |
C361F |
probably damaging |
Het |
Ppp4r4 |
T |
C |
12: 103,567,619 (GRCm39) |
|
probably benign |
Het |
Pramel26 |
T |
A |
4: 143,538,269 (GRCm39) |
D234V |
probably benign |
Het |
Prdm10 |
G |
A |
9: 31,260,564 (GRCm39) |
|
probably null |
Het |
Prex2 |
T |
A |
1: 11,159,930 (GRCm39) |
|
probably null |
Het |
Prss56 |
T |
G |
1: 87,112,452 (GRCm39) |
|
probably null |
Het |
Prtg |
A |
G |
9: 72,752,240 (GRCm39) |
K209E |
probably benign |
Het |
Ptprc |
G |
A |
1: 138,050,313 (GRCm39) |
T36I |
possibly damaging |
Het |
Rasgrp4 |
A |
G |
7: 28,845,285 (GRCm39) |
Y302C |
probably damaging |
Het |
Rb1cc1 |
T |
A |
1: 6,318,858 (GRCm39) |
M759K |
probably damaging |
Het |
Rbm15b |
T |
A |
9: 106,763,197 (GRCm39) |
M324L |
probably benign |
Het |
Rcbtb2 |
T |
C |
14: 73,415,987 (GRCm39) |
V500A |
probably damaging |
Het |
Rgs6 |
A |
G |
12: 83,180,451 (GRCm39) |
K434R |
probably damaging |
Het |
Rims1 |
C |
T |
1: 22,635,607 (GRCm39) |
A125T |
possibly damaging |
Het |
Robo3 |
A |
G |
9: 37,333,473 (GRCm39) |
V746A |
probably benign |
Het |
Rtl1 |
C |
T |
12: 109,557,820 (GRCm39) |
E1340K |
unknown |
Het |
Sacs |
G |
A |
14: 61,443,089 (GRCm39) |
D1712N |
possibly damaging |
Het |
Samd4b |
G |
A |
7: 28,103,402 (GRCm39) |
P19S |
probably benign |
Het |
Samhd1 |
T |
C |
2: 156,956,151 (GRCm39) |
Y347C |
probably damaging |
Het |
Sema6d |
T |
A |
2: 124,500,410 (GRCm39) |
I393N |
probably damaging |
Het |
Sigmar1 |
C |
T |
4: 41,741,243 (GRCm39) |
A4T |
probably benign |
Het |
Skint9 |
C |
A |
4: 112,246,376 (GRCm39) |
L245F |
probably benign |
Het |
Slc35f5 |
T |
C |
1: 125,512,832 (GRCm39) |
L372P |
probably damaging |
Het |
Smc1b |
A |
T |
15: 84,950,478 (GRCm39) |
I1182N |
probably damaging |
Het |
Smyd3 |
A |
G |
1: 178,785,138 (GRCm39) |
|
probably benign |
Het |
Sptlc1 |
T |
C |
13: 53,491,648 (GRCm39) |
D417G |
probably benign |
Het |
Sv2c |
T |
C |
13: 96,225,216 (GRCm39) |
N31S |
probably benign |
Het |
Tjp1 |
T |
C |
7: 64,964,738 (GRCm39) |
D811G |
probably damaging |
Het |
Top2b |
A |
G |
14: 16,418,442 (GRCm38) |
T1221A |
probably benign |
Het |
Tph2 |
T |
C |
10: 115,010,014 (GRCm39) |
D182G |
probably damaging |
Het |
Traf6 |
C |
T |
2: 101,518,933 (GRCm39) |
Q141* |
probably null |
Het |
Ttn |
T |
C |
2: 76,587,275 (GRCm39) |
D21574G |
probably damaging |
Het |
Uba2 |
T |
A |
7: 33,850,446 (GRCm39) |
N367I |
probably benign |
Het |
Ube2b |
T |
C |
11: 51,879,429 (GRCm39) |
|
probably benign |
Het |
Ubr5 |
G |
T |
15: 38,030,916 (GRCm39) |
L426I |
probably benign |
Het |
Ugt2a2 |
T |
A |
5: 87,612,007 (GRCm39) |
H301L |
probably benign |
Het |
Upf2 |
T |
A |
2: 6,023,705 (GRCm39) |
|
probably benign |
Het |
Vmn2r25 |
T |
C |
6: 123,800,140 (GRCm39) |
D734G |
probably damaging |
Het |
Vmn2r68 |
C |
G |
7: 84,882,466 (GRCm39) |
|
probably null |
Het |
Vmn2r68 |
T |
A |
7: 84,882,457 (GRCm39) |
|
probably benign |
Het |
Vwf |
T |
A |
6: 125,603,324 (GRCm39) |
Y891* |
probably null |
Het |
Wwox |
C |
T |
8: 115,433,018 (GRCm39) |
T228I |
probably benign |
Het |
Zer1 |
C |
T |
2: 29,998,225 (GRCm39) |
|
probably benign |
Het |
Zfp180 |
C |
T |
7: 23,804,132 (GRCm39) |
H184Y |
possibly damaging |
Het |
Zfp68 |
A |
T |
5: 138,605,487 (GRCm39) |
Y279N |
probably benign |
Het |
|
Other mutations in Utrn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00333:Utrn
|
APN |
10 |
12,547,574 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00469:Utrn
|
APN |
10 |
12,282,273 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00518:Utrn
|
APN |
10 |
12,542,587 (GRCm39) |
splice site |
probably benign |
|
IGL00560:Utrn
|
APN |
10 |
12,331,211 (GRCm39) |
nonsense |
probably null |
|
IGL00589:Utrn
|
APN |
10 |
12,554,362 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL00662:Utrn
|
APN |
10 |
12,540,705 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00754:Utrn
|
APN |
10 |
12,539,236 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00772:Utrn
|
APN |
10 |
12,524,929 (GRCm39) |
missense |
probably benign |
|
IGL00775:Utrn
|
APN |
10 |
12,620,974 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00782:Utrn
|
APN |
10 |
12,528,555 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00962:Utrn
|
APN |
10 |
12,357,078 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01584:Utrn
|
APN |
10 |
12,602,111 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01677:Utrn
|
APN |
10 |
12,619,901 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01695:Utrn
|
APN |
10 |
12,621,086 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01743:Utrn
|
APN |
10 |
12,587,301 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01815:Utrn
|
APN |
10 |
12,528,460 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01901:Utrn
|
APN |
10 |
12,516,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01982:Utrn
|
APN |
10 |
12,623,773 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01983:Utrn
|
APN |
10 |
12,545,525 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02031:Utrn
|
APN |
10 |
12,610,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02106:Utrn
|
APN |
10 |
12,289,717 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02134:Utrn
|
APN |
10 |
12,519,163 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02209:Utrn
|
APN |
10 |
12,559,039 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02217:Utrn
|
APN |
10 |
12,627,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02250:Utrn
|
APN |
10 |
12,312,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02307:Utrn
|
APN |
10 |
12,625,809 (GRCm39) |
nonsense |
probably null |
|
IGL02386:Utrn
|
APN |
10 |
12,297,352 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02494:Utrn
|
APN |
10 |
12,585,798 (GRCm39) |
missense |
probably benign |
|
IGL02631:Utrn
|
APN |
10 |
12,585,807 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02729:Utrn
|
APN |
10 |
12,596,554 (GRCm39) |
unclassified |
probably benign |
|
IGL02736:Utrn
|
APN |
10 |
12,297,384 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02832:Utrn
|
APN |
10 |
12,613,937 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02926:Utrn
|
APN |
10 |
12,566,504 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03184:Utrn
|
APN |
10 |
12,585,910 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03194:Utrn
|
APN |
10 |
12,282,173 (GRCm39) |
splice site |
probably benign |
|
IGL03346:Utrn
|
APN |
10 |
12,401,096 (GRCm39) |
missense |
probably benign |
0.22 |
retiring
|
UTSW |
10 |
12,516,764 (GRCm39) |
missense |
probably damaging |
1.00 |
shrinking_violet
|
UTSW |
10 |
12,587,329 (GRCm39) |
critical splice acceptor site |
probably null |
|
Wallflower
|
UTSW |
10 |
12,623,719 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4548:Utrn
|
UTSW |
10 |
12,509,685 (GRCm39) |
critical splice donor site |
probably benign |
|
I2288:Utrn
|
UTSW |
10 |
12,297,384 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4677001:Utrn
|
UTSW |
10 |
12,542,448 (GRCm39) |
missense |
probably benign |
0.06 |
R0022:Utrn
|
UTSW |
10 |
12,585,700 (GRCm39) |
splice site |
probably benign |
|
R0024:Utrn
|
UTSW |
10 |
12,281,755 (GRCm39) |
missense |
probably benign |
0.00 |
R0024:Utrn
|
UTSW |
10 |
12,281,755 (GRCm39) |
missense |
probably benign |
0.00 |
R0026:Utrn
|
UTSW |
10 |
12,601,940 (GRCm39) |
splice site |
probably benign |
|
R0026:Utrn
|
UTSW |
10 |
12,601,940 (GRCm39) |
splice site |
probably benign |
|
R0091:Utrn
|
UTSW |
10 |
12,610,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R0112:Utrn
|
UTSW |
10 |
12,562,209 (GRCm39) |
nonsense |
probably null |
|
R0126:Utrn
|
UTSW |
10 |
12,587,219 (GRCm39) |
missense |
probably benign |
0.02 |
R0184:Utrn
|
UTSW |
10 |
12,543,362 (GRCm39) |
missense |
probably benign |
|
R0219:Utrn
|
UTSW |
10 |
12,560,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Utrn
|
UTSW |
10 |
12,509,766 (GRCm39) |
missense |
probably benign |
0.37 |
R0391:Utrn
|
UTSW |
10 |
12,401,077 (GRCm39) |
splice site |
probably benign |
|
R0408:Utrn
|
UTSW |
10 |
12,259,934 (GRCm39) |
makesense |
probably null |
|
R0409:Utrn
|
UTSW |
10 |
12,519,345 (GRCm39) |
missense |
probably benign |
0.01 |
R0441:Utrn
|
UTSW |
10 |
12,564,038 (GRCm39) |
missense |
probably null |
0.88 |
R0504:Utrn
|
UTSW |
10 |
12,278,639 (GRCm39) |
missense |
probably benign |
0.02 |
R0730:Utrn
|
UTSW |
10 |
12,573,902 (GRCm39) |
splice site |
probably benign |
|
R1078:Utrn
|
UTSW |
10 |
12,331,310 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1171:Utrn
|
UTSW |
10 |
12,357,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R1191:Utrn
|
UTSW |
10 |
12,509,777 (GRCm39) |
missense |
probably benign |
0.02 |
R1203:Utrn
|
UTSW |
10 |
12,362,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Utrn
|
UTSW |
10 |
12,524,897 (GRCm39) |
missense |
probably benign |
|
R1418:Utrn
|
UTSW |
10 |
12,589,094 (GRCm39) |
missense |
probably benign |
|
R1439:Utrn
|
UTSW |
10 |
12,619,793 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1441:Utrn
|
UTSW |
10 |
12,559,039 (GRCm39) |
missense |
probably damaging |
0.97 |
R1445:Utrn
|
UTSW |
10 |
12,554,318 (GRCm39) |
splice site |
probably benign |
|
R1509:Utrn
|
UTSW |
10 |
12,331,185 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1546:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Utrn
|
UTSW |
10 |
12,312,029 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1621:Utrn
|
UTSW |
10 |
12,589,027 (GRCm39) |
missense |
probably benign |
0.24 |
R1637:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Utrn
|
UTSW |
10 |
12,603,473 (GRCm39) |
splice site |
probably benign |
|
R1725:Utrn
|
UTSW |
10 |
12,539,263 (GRCm39) |
missense |
probably damaging |
0.99 |
R1735:Utrn
|
UTSW |
10 |
12,585,882 (GRCm39) |
missense |
probably benign |
|
R1770:Utrn
|
UTSW |
10 |
12,351,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R1778:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Utrn
|
UTSW |
10 |
12,339,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Utrn
|
UTSW |
10 |
12,585,708 (GRCm39) |
critical splice donor site |
probably null |
|
R1829:Utrn
|
UTSW |
10 |
12,351,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Utrn
|
UTSW |
10 |
12,331,224 (GRCm39) |
missense |
probably benign |
0.15 |
R1964:Utrn
|
UTSW |
10 |
12,560,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Utrn
|
UTSW |
10 |
12,612,826 (GRCm39) |
missense |
probably benign |
0.36 |
R2092:Utrn
|
UTSW |
10 |
12,554,442 (GRCm39) |
missense |
probably benign |
0.12 |
R2107:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R2760:Utrn
|
UTSW |
10 |
12,566,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R2884:Utrn
|
UTSW |
10 |
12,615,105 (GRCm39) |
splice site |
probably null |
|
R2885:Utrn
|
UTSW |
10 |
12,615,105 (GRCm39) |
splice site |
probably null |
|
R2886:Utrn
|
UTSW |
10 |
12,615,105 (GRCm39) |
splice site |
probably null |
|
R2903:Utrn
|
UTSW |
10 |
12,519,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R2944:Utrn
|
UTSW |
10 |
12,519,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R2945:Utrn
|
UTSW |
10 |
12,362,135 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3438:Utrn
|
UTSW |
10 |
12,357,062 (GRCm39) |
missense |
probably damaging |
0.98 |
R3683:Utrn
|
UTSW |
10 |
12,542,579 (GRCm39) |
missense |
probably benign |
0.10 |
R3735:Utrn
|
UTSW |
10 |
12,354,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Utrn
|
UTSW |
10 |
12,585,926 (GRCm39) |
splice site |
probably benign |
|
R3923:Utrn
|
UTSW |
10 |
12,615,223 (GRCm39) |
missense |
probably benign |
0.23 |
R3925:Utrn
|
UTSW |
10 |
12,573,786 (GRCm39) |
missense |
probably benign |
|
R3926:Utrn
|
UTSW |
10 |
12,573,786 (GRCm39) |
missense |
probably benign |
|
R3938:Utrn
|
UTSW |
10 |
12,625,774 (GRCm39) |
critical splice donor site |
probably null |
|
R3941:Utrn
|
UTSW |
10 |
12,587,329 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3958:Utrn
|
UTSW |
10 |
12,625,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Utrn
|
UTSW |
10 |
12,585,915 (GRCm39) |
missense |
probably benign |
0.10 |
R4454:Utrn
|
UTSW |
10 |
12,603,584 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4585:Utrn
|
UTSW |
10 |
12,564,050 (GRCm39) |
missense |
probably benign |
0.01 |
R4667:Utrn
|
UTSW |
10 |
12,573,797 (GRCm39) |
missense |
probably benign |
0.22 |
R4684:Utrn
|
UTSW |
10 |
12,620,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R4782:Utrn
|
UTSW |
10 |
12,625,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Utrn
|
UTSW |
10 |
12,530,489 (GRCm39) |
missense |
probably benign |
0.39 |
R4799:Utrn
|
UTSW |
10 |
12,625,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Utrn
|
UTSW |
10 |
12,539,205 (GRCm39) |
missense |
probably benign |
0.00 |
R4878:Utrn
|
UTSW |
10 |
12,603,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Utrn
|
UTSW |
10 |
12,737,311 (GRCm39) |
critical splice donor site |
probably null |
|
R4967:Utrn
|
UTSW |
10 |
12,331,164 (GRCm39) |
missense |
probably damaging |
0.99 |
R5071:Utrn
|
UTSW |
10 |
12,259,948 (GRCm39) |
splice site |
probably null |
|
R5072:Utrn
|
UTSW |
10 |
12,259,948 (GRCm39) |
splice site |
probably null |
|
R5186:Utrn
|
UTSW |
10 |
12,604,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Utrn
|
UTSW |
10 |
12,512,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R5296:Utrn
|
UTSW |
10 |
12,277,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Utrn
|
UTSW |
10 |
12,603,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5312:Utrn
|
UTSW |
10 |
12,603,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Utrn
|
UTSW |
10 |
12,516,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R5407:Utrn
|
UTSW |
10 |
12,556,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5411:Utrn
|
UTSW |
10 |
12,524,929 (GRCm39) |
missense |
probably benign |
|
R5428:Utrn
|
UTSW |
10 |
12,569,175 (GRCm39) |
missense |
probably benign |
0.09 |
R5595:Utrn
|
UTSW |
10 |
12,558,062 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5602:Utrn
|
UTSW |
10 |
12,625,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5608:Utrn
|
UTSW |
10 |
12,547,581 (GRCm39) |
missense |
probably benign |
0.00 |
R5678:Utrn
|
UTSW |
10 |
12,317,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Utrn
|
UTSW |
10 |
12,545,550 (GRCm39) |
missense |
probably benign |
|
R5804:Utrn
|
UTSW |
10 |
12,297,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Utrn
|
UTSW |
10 |
12,540,795 (GRCm39) |
missense |
probably damaging |
0.97 |
R5941:Utrn
|
UTSW |
10 |
12,362,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Utrn
|
UTSW |
10 |
12,566,620 (GRCm39) |
missense |
probably benign |
0.01 |
R6015:Utrn
|
UTSW |
10 |
12,354,168 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6028:Utrn
|
UTSW |
10 |
12,530,460 (GRCm39) |
missense |
probably benign |
0.00 |
R6158:Utrn
|
UTSW |
10 |
12,566,566 (GRCm39) |
missense |
probably benign |
0.04 |
R6181:Utrn
|
UTSW |
10 |
12,615,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6300:Utrn
|
UTSW |
10 |
12,377,220 (GRCm39) |
missense |
probably benign |
0.35 |
R6367:Utrn
|
UTSW |
10 |
12,623,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R6377:Utrn
|
UTSW |
10 |
12,619,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Utrn
|
UTSW |
10 |
12,401,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6498:Utrn
|
UTSW |
10 |
12,317,837 (GRCm39) |
missense |
probably benign |
|
R6579:Utrn
|
UTSW |
10 |
12,623,750 (GRCm39) |
missense |
probably benign |
0.05 |
R6704:Utrn
|
UTSW |
10 |
12,621,035 (GRCm39) |
missense |
probably damaging |
0.99 |
R6736:Utrn
|
UTSW |
10 |
12,497,047 (GRCm39) |
missense |
probably benign |
0.09 |
R6755:Utrn
|
UTSW |
10 |
12,574,831 (GRCm39) |
missense |
probably benign |
0.00 |
R6793:Utrn
|
UTSW |
10 |
12,574,844 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6793:Utrn
|
UTSW |
10 |
12,516,669 (GRCm39) |
critical splice donor site |
probably null |
|
R6835:Utrn
|
UTSW |
10 |
12,603,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6919:Utrn
|
UTSW |
10 |
12,569,214 (GRCm39) |
nonsense |
probably null |
|
R6920:Utrn
|
UTSW |
10 |
12,626,214 (GRCm39) |
missense |
probably damaging |
0.98 |
R7037:Utrn
|
UTSW |
10 |
12,702,514 (GRCm39) |
splice site |
probably null |
|
R7038:Utrn
|
UTSW |
10 |
12,558,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R7055:Utrn
|
UTSW |
10 |
12,623,665 (GRCm39) |
missense |
probably benign |
0.23 |
R7072:Utrn
|
UTSW |
10 |
12,340,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R7090:Utrn
|
UTSW |
10 |
12,560,260 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7211:Utrn
|
UTSW |
10 |
12,277,079 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7248:Utrn
|
UTSW |
10 |
12,604,562 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7305:Utrn
|
UTSW |
10 |
12,261,280 (GRCm39) |
missense |
probably benign |
|
R7334:Utrn
|
UTSW |
10 |
12,603,753 (GRCm39) |
splice site |
probably null |
|
R7348:Utrn
|
UTSW |
10 |
12,623,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Utrn
|
UTSW |
10 |
12,516,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7436:Utrn
|
UTSW |
10 |
12,315,535 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7476:Utrn
|
UTSW |
10 |
12,516,695 (GRCm39) |
missense |
probably benign |
|
R7514:Utrn
|
UTSW |
10 |
12,573,833 (GRCm39) |
missense |
probably benign |
0.00 |
R7527:Utrn
|
UTSW |
10 |
12,277,126 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7735:Utrn
|
UTSW |
10 |
12,619,787 (GRCm39) |
critical splice donor site |
probably null |
|
R7748:Utrn
|
UTSW |
10 |
12,490,252 (GRCm39) |
missense |
probably benign |
0.01 |
R7778:Utrn
|
UTSW |
10 |
12,362,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7824:Utrn
|
UTSW |
10 |
12,362,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7826:Utrn
|
UTSW |
10 |
12,277,050 (GRCm39) |
splice site |
probably null |
|
R7872:Utrn
|
UTSW |
10 |
12,573,873 (GRCm39) |
missense |
probably benign |
|
R7915:Utrn
|
UTSW |
10 |
12,340,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Utrn
|
UTSW |
10 |
12,543,271 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8081:Utrn
|
UTSW |
10 |
12,423,803 (GRCm39) |
start gained |
probably benign |
|
R8132:Utrn
|
UTSW |
10 |
12,558,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R8167:Utrn
|
UTSW |
10 |
12,547,558 (GRCm39) |
nonsense |
probably null |
|
R8186:Utrn
|
UTSW |
10 |
12,573,867 (GRCm39) |
missense |
probably benign |
|
R8331:Utrn
|
UTSW |
10 |
12,490,363 (GRCm39) |
missense |
probably benign |
0.00 |
R8352:Utrn
|
UTSW |
10 |
12,689,253 (GRCm39) |
missense |
probably benign |
0.34 |
R8408:Utrn
|
UTSW |
10 |
12,545,887 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8452:Utrn
|
UTSW |
10 |
12,689,253 (GRCm39) |
missense |
probably benign |
0.34 |
R8478:Utrn
|
UTSW |
10 |
12,524,892 (GRCm39) |
missense |
probably benign |
|
R8489:Utrn
|
UTSW |
10 |
12,587,190 (GRCm39) |
missense |
probably benign |
0.05 |
R8516:Utrn
|
UTSW |
10 |
12,362,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R8520:Utrn
|
UTSW |
10 |
12,545,930 (GRCm39) |
nonsense |
probably null |
|
R8550:Utrn
|
UTSW |
10 |
12,689,329 (GRCm39) |
intron |
probably benign |
|
R8856:Utrn
|
UTSW |
10 |
12,543,351 (GRCm39) |
missense |
probably benign |
|
R8881:Utrn
|
UTSW |
10 |
12,423,737 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9180:Utrn
|
UTSW |
10 |
12,545,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R9186:Utrn
|
UTSW |
10 |
12,490,318 (GRCm39) |
missense |
probably benign |
|
R9216:Utrn
|
UTSW |
10 |
12,689,229 (GRCm39) |
missense |
probably benign |
0.19 |
R9251:Utrn
|
UTSW |
10 |
12,512,531 (GRCm39) |
missense |
probably benign |
0.01 |
R9273:Utrn
|
UTSW |
10 |
12,509,707 (GRCm39) |
missense |
probably damaging |
0.97 |
R9307:Utrn
|
UTSW |
10 |
12,554,475 (GRCm39) |
missense |
probably benign |
0.02 |
R9344:Utrn
|
UTSW |
10 |
12,560,275 (GRCm39) |
missense |
probably benign |
0.17 |
R9419:Utrn
|
UTSW |
10 |
12,564,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R9435:Utrn
|
UTSW |
10 |
12,519,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R9623:Utrn
|
UTSW |
10 |
12,282,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Utrn
|
UTSW |
10 |
12,613,929 (GRCm39) |
missense |
probably benign |
0.00 |
R9653:Utrn
|
UTSW |
10 |
12,539,189 (GRCm39) |
missense |
probably benign |
0.41 |
R9653:Utrn
|
UTSW |
10 |
12,497,123 (GRCm39) |
missense |
probably benign |
0.17 |
R9672:Utrn
|
UTSW |
10 |
12,603,613 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9678:Utrn
|
UTSW |
10 |
12,615,159 (GRCm39) |
missense |
probably benign |
0.00 |
R9741:Utrn
|
UTSW |
10 |
12,702,564 (GRCm39) |
missense |
probably benign |
|
R9765:Utrn
|
UTSW |
10 |
12,610,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R9799:Utrn
|
UTSW |
10 |
12,585,736 (GRCm39) |
missense |
probably benign |
0.01 |
RF009:Utrn
|
UTSW |
10 |
12,509,689 (GRCm39) |
nonsense |
probably null |
|
V1662:Utrn
|
UTSW |
10 |
12,297,384 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Utrn
|
UTSW |
10 |
12,610,942 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Utrn
|
UTSW |
10 |
12,564,173 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Utrn
|
UTSW |
10 |
12,558,104 (GRCm39) |
nonsense |
probably null |
|
Z1177:Utrn
|
UTSW |
10 |
12,497,123 (GRCm39) |
missense |
probably benign |
0.17 |
Z1177:Utrn
|
UTSW |
10 |
12,401,150 (GRCm39) |
nonsense |
probably null |
|
Z1186:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1189:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1191:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1192:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
|