Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
C |
T |
6: 83,138,654 (GRCm39) |
A193V |
probably benign |
Het |
Aatf |
C |
T |
11: 84,340,006 (GRCm39) |
R435Q |
probably damaging |
Het |
Abca13 |
A |
G |
11: 9,248,854 (GRCm39) |
H2867R |
probably benign |
Het |
Abcd2 |
C |
T |
15: 91,043,326 (GRCm39) |
A621T |
possibly damaging |
Het |
Actl11 |
T |
A |
9: 107,805,856 (GRCm39) |
S60T |
probably damaging |
Het |
Adam28 |
T |
A |
14: 68,874,846 (GRCm39) |
N277I |
probably damaging |
Het |
Adamts13 |
T |
A |
2: 26,896,326 (GRCm39) |
C1240S |
probably damaging |
Het |
Arhgap27 |
C |
T |
11: 103,251,581 (GRCm39) |
R49Q |
probably damaging |
Het |
Armc10 |
T |
C |
5: 21,865,581 (GRCm39) |
S209P |
probably damaging |
Het |
Atp6v0a1 |
T |
C |
11: 100,934,783 (GRCm39) |
F617L |
probably benign |
Het |
Bap1 |
T |
A |
14: 30,973,580 (GRCm39) |
N2K |
probably damaging |
Het |
Bltp1 |
C |
A |
3: 37,102,158 (GRCm39) |
N1363K |
|
Het |
Cass4 |
T |
A |
2: 172,269,106 (GRCm39) |
L396* |
probably null |
Het |
Ccdc40 |
A |
G |
11: 119,155,270 (GRCm39) |
Q1170R |
probably damaging |
Het |
Cdhr5 |
C |
T |
7: 140,852,572 (GRCm39) |
R348H |
probably damaging |
Het |
Cenpj |
A |
G |
14: 56,790,109 (GRCm39) |
S647P |
probably benign |
Het |
Chordc1 |
T |
A |
9: 18,206,647 (GRCm39) |
|
probably null |
Het |
Chordc1 |
T |
C |
9: 18,212,308 (GRCm39) |
S41P |
probably damaging |
Het |
Ckm |
T |
C |
7: 19,148,978 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
A |
C |
3: 144,711,727 (GRCm39) |
I756S |
probably damaging |
Het |
Clcn1 |
T |
C |
6: 42,268,323 (GRCm39) |
V165A |
possibly damaging |
Het |
Clec4a4 |
T |
A |
6: 122,968,704 (GRCm39) |
|
probably null |
Het |
Cog7 |
T |
C |
7: 121,576,537 (GRCm39) |
K130E |
probably damaging |
Het |
Coq7 |
A |
G |
7: 118,109,271 (GRCm39) |
I259T |
unknown |
Het |
Cp |
T |
C |
3: 20,029,130 (GRCm39) |
S536P |
probably damaging |
Het |
Cyp2d10 |
T |
A |
15: 82,288,447 (GRCm39) |
|
probably null |
Het |
Dcst2 |
A |
G |
3: 89,273,607 (GRCm39) |
I162V |
probably benign |
Het |
Dennd4c |
A |
G |
4: 86,721,228 (GRCm39) |
E630G |
probably damaging |
Het |
Dpt |
A |
T |
1: 164,624,484 (GRCm39) |
I62F |
probably benign |
Het |
Ednrb |
T |
A |
14: 104,080,444 (GRCm39) |
I157F |
probably damaging |
Het |
Ext1 |
A |
T |
15: 53,208,558 (GRCm39) |
W68R |
probably benign |
Het |
Fgf4 |
A |
G |
7: 144,416,523 (GRCm39) |
K152E |
probably benign |
Het |
G530012D18Rik |
A |
T |
1: 85,504,864 (GRCm39) |
T90S |
unknown |
Het |
Galnt17 |
T |
C |
5: 130,992,949 (GRCm39) |
T322A |
possibly damaging |
Het |
Gcm1 |
A |
T |
9: 77,966,925 (GRCm39) |
D48V |
possibly damaging |
Het |
Gdi1 |
G |
A |
X: 73,350,461 (GRCm39) |
R55H |
probably benign |
Het |
Gm49358 |
G |
T |
10: 86,661,071 (GRCm39) |
R353L |
probably damaging |
Het |
Golga4 |
A |
G |
9: 118,365,908 (GRCm39) |
E320G |
possibly damaging |
Het |
Herc3 |
T |
C |
6: 58,895,758 (GRCm39) |
I1002T |
probably damaging |
Het |
Hip1r |
T |
A |
5: 124,111,845 (GRCm39) |
V7E |
possibly damaging |
Het |
Hipk1 |
G |
A |
3: 103,684,926 (GRCm39) |
Q230* |
probably null |
Het |
Igsf9b |
C |
T |
9: 27,242,992 (GRCm39) |
P726L |
probably damaging |
Het |
Itgb6 |
T |
C |
2: 60,464,998 (GRCm39) |
I345V |
probably damaging |
Het |
Lhx4 |
G |
T |
1: 155,600,699 (GRCm39) |
Q29K |
probably benign |
Het |
Manba |
A |
G |
3: 135,273,396 (GRCm39) |
T777A |
probably benign |
Het |
Mcm3ap |
A |
G |
10: 76,337,145 (GRCm39) |
D1360G |
probably benign |
Het |
Meltf |
T |
A |
16: 31,709,632 (GRCm39) |
|
probably null |
Het |
Mmp14 |
T |
G |
14: 54,673,336 (GRCm39) |
D81E |
probably damaging |
Het |
Naalad2 |
T |
C |
9: 18,275,337 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Or7a38 |
A |
T |
10: 78,753,339 (GRCm39) |
I222L |
possibly damaging |
Het |
Or8b35 |
T |
A |
9: 37,904,253 (GRCm39) |
M150K |
possibly damaging |
Het |
Pacs2 |
A |
G |
12: 113,025,312 (GRCm39) |
D488G |
possibly damaging |
Het |
Prr5 |
T |
G |
15: 84,629,993 (GRCm39) |
L108R |
probably null |
Het |
Psg23 |
A |
G |
7: 18,341,064 (GRCm39) |
S397P |
probably benign |
Het |
Rfpl4 |
C |
A |
7: 5,113,659 (GRCm39) |
R174L |
probably damaging |
Het |
Runx3 |
T |
A |
4: 134,880,090 (GRCm39) |
I3N |
probably damaging |
Het |
Scn5a |
A |
T |
9: 119,372,451 (GRCm39) |
N214K |
possibly damaging |
Het |
Slc27a1 |
T |
C |
8: 72,037,092 (GRCm39) |
I412T |
probably damaging |
Het |
Sptbn4 |
T |
G |
7: 27,116,210 (GRCm39) |
T530P |
probably benign |
Het |
Tmod1 |
A |
T |
4: 46,093,951 (GRCm39) |
K221* |
probably null |
Het |
Tpm3 |
G |
A |
3: 89,998,361 (GRCm39) |
D272N |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,831,155 (GRCm39) |
V1340A |
probably benign |
Het |
Ugt2b5 |
A |
T |
5: 87,273,131 (GRCm39) |
C512S |
probably benign |
Het |
Vmn2r82 |
A |
T |
10: 79,215,268 (GRCm39) |
E417V |
probably benign |
Het |
Wfdc11 |
T |
C |
2: 164,506,366 (GRCm39) |
N60S |
probably benign |
Het |
Zfp217 |
A |
T |
2: 169,956,072 (GRCm39) |
S975R |
probably benign |
Het |
Zfr |
C |
T |
15: 12,146,309 (GRCm39) |
Q287* |
probably null |
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 |
34,060,854 (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 |
R9574:Tex15
|
UTSW |
8 |
34,064,509 (GRCm39) |
missense |
probably benign |
0.09 |
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 |
|