Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik1 |
T |
A |
11: 48,838,496 (GRCm39) |
E697V |
probably damaging |
Het |
Actn4 |
T |
C |
7: 28,594,864 (GRCm39) |
D805G |
probably benign |
Het |
Adam2 |
C |
T |
14: 66,275,071 (GRCm39) |
S554N |
probably benign |
Het |
Adra2b |
A |
G |
2: 127,206,283 (GRCm39) |
T267A |
probably benign |
Het |
Apobec4 |
A |
T |
1: 152,632,415 (GRCm39) |
T148S |
probably damaging |
Het |
B4galt1 |
T |
A |
4: 40,853,766 (GRCm39) |
M14L |
probably benign |
Het |
Bok |
C |
A |
1: 93,616,947 (GRCm39) |
Q98K |
probably benign |
Het |
Cacnb4 |
A |
T |
2: 52,327,016 (GRCm39) |
L394Q |
probably damaging |
Het |
Ccar2 |
T |
C |
14: 70,381,105 (GRCm39) |
K287E |
probably benign |
Het |
Cdyl2 |
T |
A |
8: 117,350,669 (GRCm39) |
E154V |
probably benign |
Het |
Cenpn |
T |
G |
8: 117,660,149 (GRCm39) |
Y160D |
probably damaging |
Het |
Cfap20 |
T |
C |
8: 96,149,514 (GRCm39) |
Y58C |
probably benign |
Het |
Creb5 |
T |
A |
6: 53,658,039 (GRCm39) |
L123Q |
unknown |
Het |
Cspg4 |
G |
A |
9: 56,797,342 (GRCm39) |
V1269M |
probably damaging |
Het |
Cyp2b19 |
G |
T |
7: 26,466,353 (GRCm39) |
K385N |
probably null |
Het |
Cyp2b19 |
A |
T |
7: 26,466,352 (GRCm39) |
K385M |
probably damaging |
Het |
Ercc2 |
C |
A |
7: 19,124,060 (GRCm39) |
D422E |
probably benign |
Het |
Fbxl12 |
A |
G |
9: 20,550,109 (GRCm39) |
V129A |
possibly damaging |
Het |
Fbxo11 |
T |
C |
17: 88,321,951 (GRCm39) |
E84G |
|
Het |
Fmn1 |
T |
C |
2: 113,425,402 (GRCm39) |
L1192S |
probably damaging |
Het |
Galk2 |
T |
C |
2: 125,824,979 (GRCm39) |
F392L |
probably benign |
Het |
Gas2l3 |
G |
A |
10: 89,258,135 (GRCm39) |
H153Y |
probably damaging |
Het |
Gcn1 |
A |
T |
5: 115,713,341 (GRCm39) |
K101N |
possibly damaging |
Het |
Gmfg |
C |
T |
7: 28,145,359 (GRCm39) |
Q101* |
probably null |
Het |
Gpr108 |
C |
T |
17: 57,545,039 (GRCm39) |
C309Y |
probably damaging |
Het |
H3c8 |
T |
C |
13: 23,719,761 (GRCm39) |
L49P |
probably damaging |
Het |
Hscb |
A |
T |
5: 110,982,595 (GRCm39) |
I164N |
probably damaging |
Het |
Kifc2 |
T |
C |
15: 76,546,397 (GRCm39) |
W260R |
probably damaging |
Het |
Lrp6 |
T |
A |
6: 134,447,662 (GRCm39) |
D995V |
possibly damaging |
Het |
Lrrc1 |
T |
A |
9: 77,358,708 (GRCm39) |
I308F |
probably damaging |
Het |
Map7 |
C |
T |
10: 20,153,966 (GRCm39) |
A694V |
unknown |
Het |
Mapre2 |
A |
G |
18: 23,965,993 (GRCm39) |
D68G |
probably benign |
Het |
Mertk |
A |
T |
2: 128,593,880 (GRCm39) |
I295F |
probably benign |
Het |
Mst1 |
T |
A |
9: 107,962,053 (GRCm39) |
C690* |
probably null |
Het |
Nde1 |
A |
G |
16: 13,988,345 (GRCm39) |
E76G |
probably damaging |
Het |
Nek5 |
T |
C |
8: 22,564,040 (GRCm39) |
T597A |
probably benign |
Het |
Nup210l |
T |
C |
3: 90,117,693 (GRCm39) |
F1800L |
probably benign |
Het |
Or5c1 |
A |
G |
2: 37,222,148 (GRCm39) |
I130V |
possibly damaging |
Het |
Pdpn |
T |
A |
4: 142,997,101 (GRCm39) |
D131V |
probably benign |
Het |
Pgap6 |
T |
C |
17: 26,337,861 (GRCm39) |
V415A |
probably damaging |
Het |
Pot1a |
T |
C |
6: 25,775,718 (GRCm39) |
T118A |
possibly damaging |
Het |
Prom1 |
A |
G |
5: 44,158,179 (GRCm39) |
I843T |
probably benign |
Het |
Prrt3 |
T |
C |
6: 113,474,587 (GRCm39) |
T212A |
probably benign |
Het |
Rabgap1 |
A |
G |
2: 37,433,246 (GRCm39) |
|
probably null |
Het |
Rarb |
A |
T |
14: 16,574,858 (GRCm38) |
S53T |
probably damaging |
Het |
Rnft2 |
A |
G |
5: 118,375,330 (GRCm39) |
S140P |
probably benign |
Het |
Rxfp1 |
T |
C |
3: 79,563,581 (GRCm39) |
M362V |
probably benign |
Het |
Sall2 |
G |
A |
14: 52,551,617 (GRCm39) |
T526M |
probably damaging |
Het |
Scube1 |
T |
C |
15: 83,501,000 (GRCm39) |
D598G |
|
Het |
Sema3f |
T |
A |
9: 107,566,972 (GRCm39) |
I186F |
possibly damaging |
Het |
Shank2 |
A |
G |
7: 143,622,462 (GRCm39) |
T199A |
possibly damaging |
Het |
Sipa1l2 |
T |
A |
8: 126,169,453 (GRCm39) |
M1427L |
probably benign |
Het |
Sis |
C |
T |
3: 72,828,490 (GRCm39) |
G1195D |
probably benign |
Het |
Slc25a39 |
A |
T |
11: 102,295,390 (GRCm39) |
H193Q |
probably benign |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
Srgn |
A |
C |
10: 62,343,444 (GRCm39) |
L17R |
probably damaging |
Het |
Stard5 |
A |
G |
7: 83,281,944 (GRCm39) |
N34D |
probably benign |
Het |
Syt8 |
A |
T |
7: 141,993,203 (GRCm39) |
D220V |
probably damaging |
Het |
Tmem131l |
T |
C |
3: 83,868,911 (GRCm39) |
R155G |
probably damaging |
Het |
Tmem220 |
T |
C |
11: 66,916,093 (GRCm39) |
V30A |
probably damaging |
Het |
Tollip |
A |
G |
7: 141,445,731 (GRCm39) |
I119T |
probably damaging |
Het |
Treml4 |
G |
A |
17: 48,571,672 (GRCm39) |
G25D |
probably damaging |
Het |
Trim7 |
T |
C |
11: 48,728,460 (GRCm39) |
F36S |
probably damaging |
Het |
Txnrd3 |
T |
A |
6: 89,640,166 (GRCm39) |
C293* |
probably null |
Het |
Utp14b |
A |
G |
1: 78,643,482 (GRCm39) |
D460G |
probably benign |
Het |
Vmn2r41 |
T |
A |
7: 8,153,329 (GRCm39) |
N397Y |
probably benign |
Het |
Vmn2r67 |
T |
C |
7: 84,786,017 (GRCm39) |
I663V |
probably benign |
Het |
Zfp292 |
T |
A |
4: 34,839,460 (GRCm39) |
H135L |
probably damaging |
Het |
Zfp420 |
C |
T |
7: 29,575,480 (GRCm39) |
R567* |
probably null |
Het |
Zfp518b |
C |
T |
5: 38,830,773 (GRCm39) |
V411M |
probably benign |
Het |
Zfp638 |
T |
A |
6: 83,956,680 (GRCm39) |
D1762E |
probably damaging |
Het |
Zfp691 |
T |
A |
4: 119,028,230 (GRCm39) |
M1L |
possibly damaging |
Het |
|
Other mutations in Tex15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00639:Tex15
|
APN |
8 |
34,065,339 (GRCm39) |
missense |
probably benign |
0.18 |
IGL00705:Tex15
|
APN |
8 |
34,071,620 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00820:Tex15
|
APN |
8 |
34,069,034 (GRCm39) |
splice site |
probably benign |
|
IGL01288:Tex15
|
APN |
8 |
34,061,412 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01328:Tex15
|
APN |
8 |
34,061,424 (GRCm39) |
nonsense |
probably null |
|
IGL01359:Tex15
|
APN |
8 |
34,071,926 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01603:Tex15
|
APN |
8 |
34,063,575 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01861:Tex15
|
APN |
8 |
34,060,717 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02052:Tex15
|
APN |
8 |
34,072,493 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02560:Tex15
|
APN |
8 |
34,071,779 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02677:Tex15
|
APN |
8 |
34,061,108 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02739:Tex15
|
APN |
8 |
34,071,721 (GRCm39) |
missense |
possibly damaging |
0.68 |
Big_gulp
|
UTSW |
8 |
34,071,762 (GRCm39) |
missense |
probably damaging |
1.00 |
P0005:Tex15
|
UTSW |
8 |
34,060,896 (GRCm39) |
missense |
probably benign |
0.00 |
P0037:Tex15
|
UTSW |
8 |
34,071,608 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4377001:Tex15
|
UTSW |
8 |
34,061,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0056:Tex15
|
UTSW |
8 |
34,072,055 (GRCm39) |
missense |
probably benign |
0.00 |
R0056:Tex15
|
UTSW |
8 |
34,072,055 (GRCm39) |
missense |
probably benign |
0.00 |
R0058:Tex15
|
UTSW |
8 |
34,071,530 (GRCm39) |
splice site |
probably benign |
|
R0058:Tex15
|
UTSW |
8 |
34,071,530 (GRCm39) |
splice site |
probably benign |
|
R0595:Tex15
|
UTSW |
8 |
34,062,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Tex15
|
UTSW |
8 |
34,072,354 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0688:Tex15
|
UTSW |
8 |
34,063,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R0842:Tex15
|
UTSW |
8 |
34,061,575 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0987:Tex15
|
UTSW |
8 |
34,066,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R1084:Tex15
|
UTSW |
8 |
34,067,032 (GRCm39) |
missense |
probably benign |
0.28 |
R1183:Tex15
|
UTSW |
8 |
34,064,893 (GRCm39) |
missense |
probably benign |
0.35 |
R1186:Tex15
|
UTSW |
8 |
34,061,661 (GRCm39) |
missense |
probably benign |
0.19 |
R1378:Tex15
|
UTSW |
8 |
34,065,244 (GRCm39) |
missense |
probably damaging |
0.99 |
R1500:Tex15
|
UTSW |
8 |
34,065,120 (GRCm39) |
missense |
probably damaging |
0.96 |
R1508:Tex15
|
UTSW |
8 |
34,066,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Tex15
|
UTSW |
8 |
34,061,511 (GRCm39) |
missense |
probably damaging |
0.96 |
R1636:Tex15
|
UTSW |
8 |
34,066,415 (GRCm39) |
nonsense |
probably null |
|
R1639:Tex15
|
UTSW |
8 |
34,060,845 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1809:Tex15
|
UTSW |
8 |
34,064,262 (GRCm39) |
missense |
probably benign |
|
R1843:Tex15
|
UTSW |
8 |
34,066,682 (GRCm39) |
missense |
probably benign |
0.27 |
R2029:Tex15
|
UTSW |
8 |
34,061,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R2228:Tex15
|
UTSW |
8 |
34,061,265 (GRCm39) |
missense |
probably benign |
0.05 |
R2229:Tex15
|
UTSW |
8 |
34,061,265 (GRCm39) |
missense |
probably benign |
0.05 |
R2245:Tex15
|
UTSW |
8 |
34,061,524 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2246:Tex15
|
UTSW |
8 |
34,072,540 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2880:Tex15
|
UTSW |
8 |
34,064,935 (GRCm39) |
nonsense |
probably null |
|
R2881:Tex15
|
UTSW |
8 |
34,064,935 (GRCm39) |
nonsense |
probably null |
|
R2882:Tex15
|
UTSW |
8 |
34,064,935 (GRCm39) |
nonsense |
probably null |
|
R3001:Tex15
|
UTSW |
8 |
34,064,556 (GRCm39) |
missense |
probably benign |
0.15 |
R3002:Tex15
|
UTSW |
8 |
34,064,556 (GRCm39) |
missense |
probably benign |
0.15 |
R3020:Tex15
|
UTSW |
8 |
34,066,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R3084:Tex15
|
UTSW |
8 |
34,064,913 (GRCm39) |
missense |
probably benign |
0.11 |
R3085:Tex15
|
UTSW |
8 |
34,064,913 (GRCm39) |
missense |
probably benign |
0.11 |
R3701:Tex15
|
UTSW |
8 |
34,064,194 (GRCm39) |
missense |
probably benign |
0.00 |
R3702:Tex15
|
UTSW |
8 |
34,064,194 (GRCm39) |
missense |
probably benign |
0.00 |
R3752:Tex15
|
UTSW |
8 |
34,061,443 (GRCm39) |
missense |
probably benign |
|
R4162:Tex15
|
UTSW |
8 |
34,071,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R4231:Tex15
|
UTSW |
8 |
34,062,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R4589:Tex15
|
UTSW |
8 |
34,047,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:Tex15
|
UTSW |
8 |
34,072,525 (GRCm39) |
missense |
probably benign |
0.00 |
R4773:Tex15
|
UTSW |
8 |
34,072,760 (GRCm39) |
missense |
probably benign |
0.42 |
R4967:Tex15
|
UTSW |
8 |
34,064,498 (GRCm39) |
missense |
probably benign |
0.34 |
R5063:Tex15
|
UTSW |
8 |
34,072,638 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5121:Tex15
|
UTSW |
8 |
34,061,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R5147:Tex15
|
UTSW |
8 |
34,062,340 (GRCm39) |
nonsense |
probably null |
|
R5166:Tex15
|
UTSW |
8 |
34,066,420 (GRCm39) |
missense |
probably benign |
0.07 |
R5173:Tex15
|
UTSW |
8 |
34,061,768 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5439:Tex15
|
UTSW |
8 |
34,064,199 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5537:Tex15
|
UTSW |
8 |
34,061,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5580:Tex15
|
UTSW |
8 |
34,062,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R5588:Tex15
|
UTSW |
8 |
34,067,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Tex15
|
UTSW |
8 |
34,063,220 (GRCm39) |
missense |
probably benign |
0.01 |
R5734:Tex15
|
UTSW |
8 |
34,036,364 (GRCm39) |
missense |
probably benign |
0.01 |
R5756:Tex15
|
UTSW |
8 |
34,065,861 (GRCm39) |
missense |
probably benign |
0.17 |
R5823:Tex15
|
UTSW |
8 |
34,060,962 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6126:Tex15
|
UTSW |
8 |
34,063,591 (GRCm39) |
missense |
probably benign |
0.19 |
R6129:Tex15
|
UTSW |
8 |
34,064,158 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6276:Tex15
|
UTSW |
8 |
34,067,217 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6374:Tex15
|
UTSW |
8 |
34,065,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R6430:Tex15
|
UTSW |
8 |
34,061,329 (GRCm39) |
missense |
probably benign |
0.01 |
R6452:Tex15
|
UTSW |
8 |
34,062,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R6471:Tex15
|
UTSW |
8 |
34,071,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R6700:Tex15
|
UTSW |
8 |
34,064,917 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6918:Tex15
|
UTSW |
8 |
34,063,212 (GRCm39) |
missense |
probably benign |
0.27 |
R6958:Tex15
|
UTSW |
8 |
34,060,899 (GRCm39) |
missense |
probably benign |
0.01 |
R6970:Tex15
|
UTSW |
8 |
34,047,456 (GRCm39) |
missense |
probably benign |
0.03 |
R7059:Tex15
|
UTSW |
8 |
34,064,758 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7069:Tex15
|
UTSW |
8 |
34,060,748 (GRCm39) |
missense |
probably benign |
|
R7072:Tex15
|
UTSW |
8 |
34,065,459 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7212:Tex15
|
UTSW |
8 |
34,063,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7212:Tex15
|
UTSW |
8 |
34,060,854 (GRCm39) |
nonsense |
probably null |
|
R7216:Tex15
|
UTSW |
8 |
34,063,014 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7219:Tex15
|
UTSW |
8 |
34,036,268 (GRCm39) |
missense |
probably benign |
0.40 |
R7313:Tex15
|
UTSW |
8 |
34,064,845 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7315:Tex15
|
UTSW |
8 |
34,071,544 (GRCm39) |
missense |
probably benign |
0.01 |
R7444:Tex15
|
UTSW |
8 |
34,066,590 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7455:Tex15
|
UTSW |
8 |
34,067,025 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7643:Tex15
|
UTSW |
8 |
34,065,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R7644:Tex15
|
UTSW |
8 |
34,064,445 (GRCm39) |
missense |
probably benign |
0.01 |
R7724:Tex15
|
UTSW |
8 |
34,036,291 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7779:Tex15
|
UTSW |
8 |
34,065,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7798:Tex15
|
UTSW |
8 |
34,071,875 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7816:Tex15
|
UTSW |
8 |
34,071,683 (GRCm39) |
missense |
probably benign |
0.14 |
R7820:Tex15
|
UTSW |
8 |
34,065,090 (GRCm39) |
missense |
probably damaging |
0.98 |
R8041:Tex15
|
UTSW |
8 |
34,065,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8150:Tex15
|
UTSW |
8 |
34,063,534 (GRCm39) |
missense |
probably benign |
0.06 |
R8152:Tex15
|
UTSW |
8 |
34,062,921 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8237:Tex15
|
UTSW |
8 |
34,067,427 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8250:Tex15
|
UTSW |
8 |
34,055,233 (GRCm39) |
missense |
probably null |
0.27 |
R8264:Tex15
|
UTSW |
8 |
34,072,390 (GRCm39) |
missense |
probably benign |
0.18 |
R8279:Tex15
|
UTSW |
8 |
34,061,765 (GRCm39) |
missense |
probably damaging |
0.96 |
R8353:Tex15
|
UTSW |
8 |
34,066,899 (GRCm39) |
nonsense |
probably null |
|
R8388:Tex15
|
UTSW |
8 |
34,065,237 (GRCm39) |
missense |
probably benign |
0.00 |
R8432:Tex15
|
UTSW |
8 |
34,066,572 (GRCm39) |
missense |
probably damaging |
0.99 |
R8453:Tex15
|
UTSW |
8 |
34,066,899 (GRCm39) |
nonsense |
probably null |
|
R8489:Tex15
|
UTSW |
8 |
34,067,574 (GRCm39) |
missense |
probably benign |
0.02 |
R8670:Tex15
|
UTSW |
8 |
34,064,746 (GRCm39) |
missense |
probably benign |
0.19 |
R8703:Tex15
|
UTSW |
8 |
34,062,724 (GRCm39) |
missense |
probably benign |
0.00 |
R8871:Tex15
|
UTSW |
8 |
34,066,992 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8945:Tex15
|
UTSW |
8 |
34,064,724 (GRCm39) |
missense |
probably benign |
0.00 |
R9104:Tex15
|
UTSW |
8 |
34,060,950 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9132:Tex15
|
UTSW |
8 |
34,067,554 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9207:Tex15
|
UTSW |
8 |
34,065,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Tex15
|
UTSW |
8 |
34,064,319 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9330:Tex15
|
UTSW |
8 |
34,065,143 (GRCm39) |
missense |
probably benign |
0.01 |
R9354:Tex15
|
UTSW |
8 |
34,063,344 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9365:Tex15
|
UTSW |
8 |
34,064,564 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9440:Tex15
|
UTSW |
8 |
34,072,273 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9534:Tex15
|
UTSW |
8 |
34,060,999 (GRCm39) |
missense |
probably benign |
0.45 |
R9570:Tex15
|
UTSW |
8 |
34,067,309 (GRCm39) |
missense |
probably damaging |
0.96 |
R9618:Tex15
|
UTSW |
8 |
34,062,397 (GRCm39) |
missense |
probably benign |
0.35 |
R9655:Tex15
|
UTSW |
8 |
34,066,784 (GRCm39) |
nonsense |
probably null |
|
R9786:Tex15
|
UTSW |
8 |
34,062,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R9798:Tex15
|
UTSW |
8 |
34,062,721 (GRCm39) |
missense |
probably damaging |
0.98 |
RF005:Tex15
|
UTSW |
8 |
34,066,705 (GRCm39) |
missense |
probably benign |
0.05 |
X0020:Tex15
|
UTSW |
8 |
34,066,607 (GRCm39) |
missense |
probably benign |
0.03 |
X0065:Tex15
|
UTSW |
8 |
34,065,545 (GRCm39) |
nonsense |
probably null |
|
Z1088:Tex15
|
UTSW |
8 |
34,061,343 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1088:Tex15
|
UTSW |
8 |
34,064,898 (GRCm39) |
missense |
probably benign |
|
Z1088:Tex15
|
UTSW |
8 |
34,061,838 (GRCm39) |
missense |
possibly damaging |
0.68 |
Z1176:Tex15
|
UTSW |
8 |
34,064,754 (GRCm39) |
missense |
possibly damaging |
0.84 |
|