Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
A |
G |
2: 151,314,728 (GRCm39) |
F317L |
possibly damaging |
Het |
Abcc4 |
A |
G |
14: 118,905,811 (GRCm39) |
I85T |
probably benign |
Het |
Acoxl |
G |
T |
2: 127,917,810 (GRCm39) |
C498F |
probably damaging |
Het |
Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
Ap2a2 |
T |
G |
7: 141,210,061 (GRCm39) |
F836C |
probably damaging |
Het |
Atp2c1 |
A |
G |
9: 105,320,149 (GRCm39) |
V404A |
probably benign |
Het |
Atp7b |
G |
T |
8: 22,510,901 (GRCm39) |
A415E |
probably damaging |
Het |
Babam2 |
A |
T |
5: 31,942,927 (GRCm39) |
I71L |
possibly damaging |
Het |
Bean1 |
A |
G |
8: 104,943,606 (GRCm39) |
T54A |
probably damaging |
Het |
Cacna1b |
T |
A |
2: 24,508,330 (GRCm39) |
I1816F |
probably damaging |
Het |
Cacna1b |
C |
T |
2: 24,547,378 (GRCm39) |
G1202D |
probably damaging |
Het |
Casp8ap2 |
A |
G |
4: 32,640,554 (GRCm39) |
E536G |
probably damaging |
Het |
Cfap57 |
A |
G |
4: 118,470,262 (GRCm39) |
V206A |
probably benign |
Het |
Clca3a2 |
A |
T |
3: 144,783,640 (GRCm39) |
D658E |
probably damaging |
Het |
Cwc22 |
A |
T |
2: 77,726,653 (GRCm39) |
S809T |
probably benign |
Het |
Cyp2c54 |
C |
T |
19: 40,060,585 (GRCm39) |
R132Q |
possibly damaging |
Het |
Ddx20 |
A |
T |
3: 105,587,921 (GRCm39) |
D386E |
possibly damaging |
Het |
Ddx50 |
T |
C |
10: 62,478,632 (GRCm39) |
T185A |
probably damaging |
Het |
Decr1 |
G |
A |
4: 15,930,976 (GRCm39) |
R119* |
probably null |
Het |
Dennd4a |
T |
C |
9: 64,813,285 (GRCm39) |
S1415P |
probably benign |
Het |
Dnah12 |
A |
T |
14: 26,437,855 (GRCm39) |
I495L |
probably benign |
Het |
Dnah2 |
G |
A |
11: 69,346,799 (GRCm39) |
Q2596* |
probably null |
Het |
Dnajb13 |
A |
G |
7: 100,156,707 (GRCm39) |
L123S |
probably benign |
Het |
Drgx |
G |
T |
14: 32,369,101 (GRCm39) |
|
probably benign |
Het |
Elavl3 |
G |
A |
9: 21,948,107 (GRCm39) |
P19L |
probably benign |
Het |
Fer1l6 |
T |
C |
15: 58,443,250 (GRCm39) |
S518P |
probably benign |
Het |
Fgd3 |
T |
C |
13: 49,420,105 (GRCm39) |
S591G |
probably benign |
Het |
Galnt18 |
C |
A |
7: 111,071,271 (GRCm39) |
R566L |
probably benign |
Het |
Galnt6 |
A |
T |
15: 100,594,455 (GRCm39) |
Y525* |
probably null |
Het |
Gm10036 |
A |
T |
18: 15,966,359 (GRCm39) |
Y170F |
probably benign |
Het |
Hacd2 |
A |
G |
16: 34,842,921 (GRCm39) |
D24G |
unknown |
Het |
Idh3a |
T |
C |
9: 54,503,325 (GRCm39) |
M128T |
possibly damaging |
Het |
Ido1 |
C |
T |
8: 25,074,565 (GRCm39) |
M359I |
probably benign |
Het |
Ikbkb |
T |
C |
8: 23,171,693 (GRCm39) |
T185A |
probably damaging |
Het |
Insl6 |
C |
T |
19: 29,299,019 (GRCm39) |
G131D |
probably damaging |
Het |
Irgm1 |
A |
C |
11: 48,757,159 (GRCm39) |
S217R |
possibly damaging |
Het |
Itga11 |
T |
A |
9: 62,668,850 (GRCm39) |
Y702* |
probably null |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Kansl2 |
T |
C |
15: 98,429,724 (GRCm39) |
M103V |
probably benign |
Het |
Kcnq2 |
T |
C |
2: 180,753,836 (GRCm39) |
N258S |
possibly damaging |
Het |
Kdm5d |
A |
T |
Y: 940,624 (GRCm39) |
D1045V |
probably damaging |
Het |
Lats2 |
A |
G |
14: 57,937,049 (GRCm39) |
L480P |
probably damaging |
Het |
Lin28b |
T |
A |
10: 45,296,736 (GRCm39) |
K87N |
possibly damaging |
Het |
Lpgat1 |
T |
A |
1: 191,451,682 (GRCm39) |
W103R |
probably damaging |
Het |
Lpl |
G |
T |
8: 69,347,345 (GRCm39) |
G166C |
probably damaging |
Het |
Ly75 |
A |
T |
2: 60,182,469 (GRCm39) |
Y569N |
probably damaging |
Het |
Mcm8 |
A |
T |
2: 132,680,689 (GRCm39) |
E564D |
probably damaging |
Het |
Me2 |
G |
T |
18: 73,918,847 (GRCm39) |
N411K |
probably damaging |
Het |
Mn1 |
A |
G |
5: 111,602,652 (GRCm39) |
T1297A |
possibly damaging |
Het |
Mphosph8 |
T |
A |
14: 56,916,046 (GRCm39) |
F447L |
probably benign |
Het |
Nacad |
T |
A |
11: 6,549,169 (GRCm39) |
D1294V |
probably damaging |
Het |
Neu3 |
A |
T |
7: 99,472,615 (GRCm39) |
F41I |
probably damaging |
Het |
Nlrp6 |
G |
T |
7: 140,503,497 (GRCm39) |
L534F |
probably damaging |
Het |
Nrap |
A |
G |
19: 56,366,575 (GRCm39) |
M338T |
probably damaging |
Het |
Nuak1 |
T |
C |
10: 84,210,979 (GRCm39) |
K370E |
probably damaging |
Het |
Or10ab4 |
T |
A |
7: 107,654,647 (GRCm39) |
C153S |
probably benign |
Het |
Or4d10 |
T |
A |
19: 12,051,639 (GRCm39) |
D119V |
probably damaging |
Het |
Or5w8 |
A |
G |
2: 87,687,632 (GRCm39) |
T38A |
probably benign |
Het |
Or6c212 |
C |
T |
10: 129,558,592 (GRCm39) |
V274M |
probably damaging |
Het |
P3h3 |
T |
C |
6: 124,818,736 (GRCm39) |
S701G |
probably benign |
Het |
Pdss2 |
T |
C |
10: 43,174,908 (GRCm39) |
M138T |
possibly damaging |
Het |
Piezo1 |
C |
T |
8: 123,213,220 (GRCm39) |
E1848K |
probably benign |
Het |
Prmt3 |
T |
G |
7: 49,476,557 (GRCm39) |
S389A |
probably benign |
Het |
Prune2 |
T |
A |
19: 17,099,637 (GRCm39) |
F1714I |
probably benign |
Het |
Ptgis |
A |
G |
2: 167,067,194 (GRCm39) |
|
probably null |
Het |
Ptpn20 |
T |
C |
14: 33,336,416 (GRCm39) |
V85A |
probably benign |
Het |
Rabepk |
A |
T |
2: 34,670,669 (GRCm39) |
Y264N |
probably damaging |
Het |
Ralgapa2 |
A |
T |
2: 146,276,754 (GRCm39) |
C495* |
probably null |
Het |
Satb2 |
A |
G |
1: 56,930,327 (GRCm39) |
I232T |
probably benign |
Het |
Selenbp2 |
A |
T |
3: 94,610,856 (GRCm39) |
L307F |
probably damaging |
Het |
Sgpl1 |
T |
G |
10: 60,949,863 (GRCm39) |
Y112S |
probably damaging |
Het |
Slitrk5 |
T |
C |
14: 111,918,679 (GRCm39) |
S768P |
probably benign |
Het |
Smc3 |
T |
A |
19: 53,619,948 (GRCm39) |
Y615N |
probably damaging |
Het |
Spag17 |
A |
G |
3: 99,934,939 (GRCm39) |
N715S |
probably benign |
Het |
Spats2 |
A |
G |
15: 99,110,157 (GRCm39) |
E518G |
probably benign |
Het |
Spats2l |
A |
G |
1: 57,924,983 (GRCm39) |
H127R |
possibly damaging |
Het |
Tenm3 |
T |
A |
8: 48,731,996 (GRCm39) |
K1287* |
probably null |
Het |
Thoc1 |
T |
A |
18: 9,962,387 (GRCm39) |
S91T |
probably benign |
Het |
Thoc6 |
C |
T |
17: 23,888,911 (GRCm39) |
G166S |
probably damaging |
Het |
Tmem107 |
C |
A |
11: 68,962,087 (GRCm39) |
T42N |
possibly damaging |
Het |
Tmprss11c |
A |
G |
5: 86,385,569 (GRCm39) |
I288T |
probably damaging |
Het |
Tnrc18 |
A |
G |
5: 142,725,248 (GRCm39) |
F1827S |
unknown |
Het |
Trmt112 |
C |
A |
19: 6,887,566 (GRCm39) |
T5N |
probably damaging |
Het |
Trp53bp1 |
A |
T |
2: 121,101,027 (GRCm39) |
M57K |
probably benign |
Het |
Ttbk2 |
C |
A |
2: 120,575,631 (GRCm39) |
Q1115H |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,559,989 (GRCm39) |
E27725* |
probably null |
Het |
Ttn |
A |
G |
2: 76,774,453 (GRCm39) |
M2151T |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,384,336 (GRCm39) |
D727E |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,781,173 (GRCm39) |
T221A |
probably damaging |
Het |
Zbtb20 |
A |
G |
16: 43,439,055 (GRCm39) |
D725G |
probably damaging |
Het |
Zfp341 |
A |
T |
2: 154,468,734 (GRCm39) |
I126F |
possibly damaging |
Het |
Zfyve16 |
C |
T |
13: 92,650,402 (GRCm39) |
A861T |
probably damaging |
Het |
|
Other mutations in Akap13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Akap13
|
APN |
7 |
75,375,719 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00332:Akap13
|
APN |
7 |
75,378,667 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00481:Akap13
|
APN |
7 |
75,373,643 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00590:Akap13
|
APN |
7 |
75,260,417 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00655:Akap13
|
APN |
7 |
75,354,146 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00766:Akap13
|
APN |
7 |
75,354,260 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00818:Akap13
|
APN |
7 |
75,259,475 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00826:Akap13
|
APN |
7 |
75,327,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01014:Akap13
|
APN |
7 |
75,400,381 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01090:Akap13
|
APN |
7 |
75,316,279 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01155:Akap13
|
APN |
7 |
75,219,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01326:Akap13
|
APN |
7 |
75,375,096 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01456:Akap13
|
APN |
7 |
75,252,595 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01460:Akap13
|
APN |
7 |
75,397,594 (GRCm39) |
missense |
probably benign |
0.29 |
IGL01568:Akap13
|
APN |
7 |
75,258,270 (GRCm39) |
nonsense |
probably null |
0.00 |
IGL01610:Akap13
|
APN |
7 |
75,397,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01610:Akap13
|
APN |
7 |
75,369,928 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01615:Akap13
|
APN |
7 |
75,347,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01667:Akap13
|
APN |
7 |
75,219,767 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01705:Akap13
|
APN |
7 |
75,396,515 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02070:Akap13
|
APN |
7 |
75,316,293 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02269:Akap13
|
APN |
7 |
75,252,659 (GRCm39) |
missense |
probably benign |
|
IGL02421:Akap13
|
APN |
7 |
75,367,554 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02870:Akap13
|
APN |
7 |
75,258,936 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02944:Akap13
|
APN |
7 |
75,258,405 (GRCm39) |
missense |
probably benign |
|
IGL03051:Akap13
|
APN |
7 |
75,260,233 (GRCm39) |
nonsense |
probably null |
|
IGL03160:Akap13
|
APN |
7 |
75,380,165 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03245:Akap13
|
APN |
7 |
75,259,500 (GRCm39) |
missense |
probably damaging |
0.99 |
R0254:Akap13
|
UTSW |
7 |
75,386,352 (GRCm39) |
splice site |
probably benign |
|
R0310:Akap13
|
UTSW |
7 |
75,264,678 (GRCm39) |
missense |
probably damaging |
0.99 |
R0373:Akap13
|
UTSW |
7 |
75,380,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Akap13
|
UTSW |
7 |
75,259,677 (GRCm39) |
missense |
probably benign |
0.00 |
R0408:Akap13
|
UTSW |
7 |
75,396,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Akap13
|
UTSW |
7 |
75,264,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R0646:Akap13
|
UTSW |
7 |
75,397,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Akap13
|
UTSW |
7 |
75,261,125 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0845:Akap13
|
UTSW |
7 |
75,375,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R1004:Akap13
|
UTSW |
7 |
75,337,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R1024:Akap13
|
UTSW |
7 |
75,327,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Akap13
|
UTSW |
7 |
75,261,125 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1346:Akap13
|
UTSW |
7 |
75,259,340 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1349:Akap13
|
UTSW |
7 |
75,259,340 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1372:Akap13
|
UTSW |
7 |
75,259,340 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1387:Akap13
|
UTSW |
7 |
75,235,941 (GRCm39) |
missense |
probably damaging |
0.97 |
R1442:Akap13
|
UTSW |
7 |
75,385,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Akap13
|
UTSW |
7 |
75,378,797 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1466:Akap13
|
UTSW |
7 |
75,378,797 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1584:Akap13
|
UTSW |
7 |
75,378,797 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1696:Akap13
|
UTSW |
7 |
75,259,340 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1738:Akap13
|
UTSW |
7 |
75,326,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R1773:Akap13
|
UTSW |
7 |
75,333,199 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1785:Akap13
|
UTSW |
7 |
75,261,182 (GRCm39) |
missense |
probably benign |
0.16 |
R1786:Akap13
|
UTSW |
7 |
75,261,182 (GRCm39) |
missense |
probably benign |
0.16 |
R1791:Akap13
|
UTSW |
7 |
75,260,783 (GRCm39) |
missense |
probably benign |
0.00 |
R1819:Akap13
|
UTSW |
7 |
75,258,453 (GRCm39) |
missense |
probably benign |
0.04 |
R1879:Akap13
|
UTSW |
7 |
75,260,475 (GRCm39) |
missense |
probably benign |
0.01 |
R1989:Akap13
|
UTSW |
7 |
75,354,264 (GRCm39) |
missense |
probably benign |
0.01 |
R2016:Akap13
|
UTSW |
7 |
75,354,279 (GRCm39) |
missense |
probably damaging |
0.99 |
R2092:Akap13
|
UTSW |
7 |
75,260,318 (GRCm39) |
missense |
probably benign |
0.05 |
R2126:Akap13
|
UTSW |
7 |
75,375,052 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2131:Akap13
|
UTSW |
7 |
75,261,182 (GRCm39) |
missense |
probably benign |
0.16 |
R2132:Akap13
|
UTSW |
7 |
75,261,182 (GRCm39) |
missense |
probably benign |
0.16 |
R2133:Akap13
|
UTSW |
7 |
75,261,182 (GRCm39) |
missense |
probably benign |
0.16 |
R2251:Akap13
|
UTSW |
7 |
75,389,225 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3704:Akap13
|
UTSW |
7 |
75,316,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Akap13
|
UTSW |
7 |
75,235,929 (GRCm39) |
missense |
probably damaging |
0.98 |
R3731:Akap13
|
UTSW |
7 |
75,261,125 (GRCm39) |
missense |
probably benign |
0.39 |
R3765:Akap13
|
UTSW |
7 |
75,258,585 (GRCm39) |
missense |
probably benign |
0.04 |
R3788:Akap13
|
UTSW |
7 |
75,351,901 (GRCm39) |
critical splice donor site |
probably null |
|
R3793:Akap13
|
UTSW |
7 |
75,259,889 (GRCm39) |
missense |
probably benign |
0.00 |
R3970:Akap13
|
UTSW |
7 |
75,219,699 (GRCm39) |
nonsense |
probably null |
|
R4205:Akap13
|
UTSW |
7 |
75,260,667 (GRCm39) |
missense |
probably benign |
0.05 |
R4257:Akap13
|
UTSW |
7 |
75,261,033 (GRCm39) |
missense |
probably damaging |
0.98 |
R4374:Akap13
|
UTSW |
7 |
75,258,732 (GRCm39) |
missense |
probably damaging |
0.96 |
R4448:Akap13
|
UTSW |
7 |
75,392,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R4450:Akap13
|
UTSW |
7 |
75,392,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R4457:Akap13
|
UTSW |
7 |
75,389,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R4458:Akap13
|
UTSW |
7 |
75,389,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R4466:Akap13
|
UTSW |
7 |
75,252,521 (GRCm39) |
splice site |
probably null |
|
R4632:Akap13
|
UTSW |
7 |
75,316,301 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4667:Akap13
|
UTSW |
7 |
75,378,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R4669:Akap13
|
UTSW |
7 |
75,378,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R4671:Akap13
|
UTSW |
7 |
75,229,312 (GRCm39) |
nonsense |
probably null |
|
R4821:Akap13
|
UTSW |
7 |
75,327,255 (GRCm39) |
intron |
probably benign |
|
R4868:Akap13
|
UTSW |
7 |
75,393,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R4894:Akap13
|
UTSW |
7 |
75,375,068 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4943:Akap13
|
UTSW |
7 |
75,398,988 (GRCm39) |
missense |
probably benign |
0.22 |
R4988:Akap13
|
UTSW |
7 |
75,380,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R5119:Akap13
|
UTSW |
7 |
75,337,000 (GRCm39) |
missense |
probably damaging |
0.98 |
R5141:Akap13
|
UTSW |
7 |
75,259,362 (GRCm39) |
missense |
probably benign |
0.18 |
R5419:Akap13
|
UTSW |
7 |
75,259,991 (GRCm39) |
missense |
probably benign |
0.01 |
R5427:Akap13
|
UTSW |
7 |
75,378,617 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5429:Akap13
|
UTSW |
7 |
75,252,652 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5432:Akap13
|
UTSW |
7 |
75,252,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R5458:Akap13
|
UTSW |
7 |
75,236,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R5636:Akap13
|
UTSW |
7 |
75,354,120 (GRCm39) |
missense |
probably damaging |
0.96 |
R5643:Akap13
|
UTSW |
7 |
75,351,902 (GRCm39) |
critical splice donor site |
probably null |
|
R5898:Akap13
|
UTSW |
7 |
75,378,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R5932:Akap13
|
UTSW |
7 |
75,259,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R6135:Akap13
|
UTSW |
7 |
75,259,656 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6137:Akap13
|
UTSW |
7 |
75,327,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R6182:Akap13
|
UTSW |
7 |
75,236,028 (GRCm39) |
missense |
probably benign |
0.45 |
R6310:Akap13
|
UTSW |
7 |
75,398,941 (GRCm39) |
missense |
probably damaging |
0.99 |
R6346:Akap13
|
UTSW |
7 |
75,335,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R6466:Akap13
|
UTSW |
7 |
75,376,792 (GRCm39) |
missense |
probably benign |
0.01 |
R6605:Akap13
|
UTSW |
7 |
75,229,516 (GRCm39) |
missense |
probably damaging |
0.98 |
R6617:Akap13
|
UTSW |
7 |
75,380,111 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6621:Akap13
|
UTSW |
7 |
75,219,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R6703:Akap13
|
UTSW |
7 |
75,252,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Akap13
|
UTSW |
7 |
75,389,206 (GRCm39) |
missense |
probably benign |
0.03 |
R7069:Akap13
|
UTSW |
7 |
75,260,010 (GRCm39) |
missense |
probably benign |
0.29 |
R7116:Akap13
|
UTSW |
7 |
75,369,943 (GRCm39) |
missense |
probably benign |
0.00 |
R7158:Akap13
|
UTSW |
7 |
75,229,342 (GRCm39) |
missense |
probably damaging |
0.97 |
R7159:Akap13
|
UTSW |
7 |
75,380,327 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7467:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R7468:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R7471:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R7472:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R7477:Akap13
|
UTSW |
7 |
75,398,995 (GRCm39) |
missense |
probably benign |
|
R7636:Akap13
|
UTSW |
7 |
75,259,621 (GRCm39) |
missense |
probably benign |
0.04 |
R7650:Akap13
|
UTSW |
7 |
75,293,202 (GRCm39) |
missense |
probably benign |
0.20 |
R7671:Akap13
|
UTSW |
7 |
75,219,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R7681:Akap13
|
UTSW |
7 |
75,378,544 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7752:Akap13
|
UTSW |
7 |
75,327,006 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7784:Akap13
|
UTSW |
7 |
75,260,076 (GRCm39) |
missense |
probably benign |
0.00 |
R7816:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R7817:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R7834:Akap13
|
UTSW |
7 |
75,392,390 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7880:Akap13
|
UTSW |
7 |
75,235,964 (GRCm39) |
missense |
probably damaging |
0.97 |
R7942:Akap13
|
UTSW |
7 |
75,261,218 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8006:Akap13
|
UTSW |
7 |
75,229,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R8009:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8011:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8013:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8016:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8089:Akap13
|
UTSW |
7 |
75,260,340 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8138:Akap13
|
UTSW |
7 |
75,351,979 (GRCm39) |
splice site |
probably null |
|
R8174:Akap13
|
UTSW |
7 |
75,378,617 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8298:Akap13
|
UTSW |
7 |
75,397,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R8444:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8445:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8465:Akap13
|
UTSW |
7 |
75,376,786 (GRCm39) |
missense |
probably benign |
0.11 |
R8512:Akap13
|
UTSW |
7 |
75,260,834 (GRCm39) |
missense |
probably damaging |
0.99 |
R8523:Akap13
|
UTSW |
7 |
75,380,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8793:Akap13
|
UTSW |
7 |
75,375,076 (GRCm39) |
missense |
probably benign |
0.35 |
R8907:Akap13
|
UTSW |
7 |
75,260,456 (GRCm39) |
missense |
probably damaging |
0.99 |
R8907:Akap13
|
UTSW |
7 |
75,260,444 (GRCm39) |
missense |
probably benign |
0.08 |
R8928:Akap13
|
UTSW |
7 |
75,259,606 (GRCm39) |
missense |
probably benign |
0.00 |
R8929:Akap13
|
UTSW |
7 |
75,258,752 (GRCm39) |
missense |
probably benign |
0.00 |
R8937:Akap13
|
UTSW |
7 |
75,184,601 (GRCm39) |
critical splice donor site |
probably null |
|
R8967:Akap13
|
UTSW |
7 |
75,378,882 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8986:Akap13
|
UTSW |
7 |
75,259,074 (GRCm39) |
missense |
probably benign |
|
R9152:Akap13
|
UTSW |
7 |
75,261,033 (GRCm39) |
missense |
probably damaging |
0.98 |
R9153:Akap13
|
UTSW |
7 |
75,259,229 (GRCm39) |
missense |
probably benign |
0.00 |
R9160:Akap13
|
UTSW |
7 |
75,385,526 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9192:Akap13
|
UTSW |
7 |
75,354,249 (GRCm39) |
missense |
probably benign |
0.06 |
R9319:Akap13
|
UTSW |
7 |
75,258,836 (GRCm39) |
missense |
probably benign |
0.01 |
R9513:Akap13
|
UTSW |
7 |
75,354,275 (GRCm39) |
missense |
probably benign |
0.01 |
R9515:Akap13
|
UTSW |
7 |
75,354,275 (GRCm39) |
missense |
probably benign |
0.01 |
R9516:Akap13
|
UTSW |
7 |
75,354,275 (GRCm39) |
missense |
probably benign |
0.01 |
R9523:Akap13
|
UTSW |
7 |
75,293,193 (GRCm39) |
missense |
|
|
R9564:Akap13
|
UTSW |
7 |
75,259,161 (GRCm39) |
missense |
probably benign |
|
R9621:Akap13
|
UTSW |
7 |
75,386,090 (GRCm39) |
missense |
probably benign |
0.09 |
R9686:Akap13
|
UTSW |
7 |
75,236,084 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Akap13
|
UTSW |
7 |
75,380,300 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Akap13
|
UTSW |
7 |
75,264,753 (GRCm39) |
missense |
probably benign |
0.17 |
|