Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
A |
T |
5: 124,227,878 (GRCm39) |
V121E |
possibly damaging |
Het |
Acsbg3 |
A |
T |
17: 57,183,373 (GRCm39) |
D38V |
probably benign |
Het |
Adamts20 |
T |
A |
15: 94,277,628 (GRCm39) |
Y278F |
probably damaging |
Het |
Adcy7 |
A |
T |
8: 89,053,020 (GRCm39) |
D972V |
probably benign |
Het |
Adgrf3 |
C |
A |
5: 30,403,360 (GRCm39) |
|
probably null |
Het |
Ahdc1 |
G |
T |
4: 132,791,206 (GRCm39) |
G816C |
probably benign |
Het |
Aifm3 |
A |
G |
16: 17,319,994 (GRCm39) |
K283E |
probably benign |
Het |
Ank1 |
T |
C |
8: 23,589,678 (GRCm39) |
L593P |
probably damaging |
Het |
Apol11b |
T |
A |
15: 77,519,697 (GRCm39) |
T128S |
probably benign |
Het |
C1qtnf7 |
C |
A |
5: 43,773,427 (GRCm39) |
T235K |
probably damaging |
Het |
Camk2a |
A |
T |
18: 61,111,029 (GRCm39) |
I73F |
probably damaging |
Het |
Ccdc121rt3 |
C |
T |
5: 112,502,874 (GRCm39) |
V277M |
possibly damaging |
Het |
Cd109 |
G |
T |
9: 78,612,344 (GRCm39) |
V1244F |
possibly damaging |
Het |
Cep164 |
A |
G |
9: 45,680,761 (GRCm39) |
L1240S |
possibly damaging |
Het |
Cnga1 |
T |
A |
5: 72,761,918 (GRCm39) |
D532V |
probably damaging |
Het |
Cyp4a14 |
A |
T |
4: 115,353,297 (GRCm39) |
L5* |
probably null |
Het |
Cyp4a30b |
A |
T |
4: 115,316,588 (GRCm39) |
K405* |
probably null |
Het |
Dchs1 |
T |
C |
7: 105,403,302 (GRCm39) |
D3080G |
probably benign |
Het |
Ddx1 |
T |
C |
12: 13,287,800 (GRCm39) |
D168G |
probably damaging |
Het |
Dhx57 |
T |
G |
17: 80,553,235 (GRCm39) |
K1231Q |
probably damaging |
Het |
Dnah14 |
A |
G |
1: 181,597,670 (GRCm39) |
N3640D |
probably benign |
Het |
Dock4 |
T |
A |
12: 40,805,833 (GRCm39) |
L935Q |
probably damaging |
Het |
Dus2 |
A |
T |
8: 106,772,698 (GRCm39) |
R269S |
probably benign |
Het |
E230025N22Rik |
G |
A |
18: 36,822,161 (GRCm39) |
R201C |
possibly damaging |
Het |
Erbb3 |
G |
A |
10: 128,419,054 (GRCm39) |
T269M |
probably damaging |
Het |
Fbxo43 |
T |
C |
15: 36,162,239 (GRCm39) |
R323G |
probably damaging |
Het |
Fktn |
A |
G |
4: 53,735,061 (GRCm39) |
H233R |
probably benign |
Het |
Ftsj3 |
A |
T |
11: 106,143,077 (GRCm39) |
D412E |
probably damaging |
Het |
Fzd7 |
A |
T |
1: 59,523,703 (GRCm39) |
M529L |
probably benign |
Het |
Fzr1 |
T |
A |
10: 81,206,660 (GRCm39) |
|
probably null |
Het |
Ganc |
T |
G |
2: 120,261,086 (GRCm39) |
V257G |
possibly damaging |
Het |
Garin1a |
T |
A |
6: 29,290,423 (GRCm39) |
L267* |
probably null |
Het |
Gm4131 |
T |
C |
14: 62,702,207 (GRCm39) |
K254E |
probably damaging |
Het |
Gm7347 |
G |
T |
5: 26,262,247 (GRCm39) |
Y91* |
probably null |
Het |
Gm9857 |
G |
A |
3: 108,847,481 (GRCm39) |
|
probably benign |
Het |
Grpel1 |
T |
C |
5: 36,622,592 (GRCm39) |
S19P |
probably benign |
Het |
Gtf3c4 |
T |
C |
2: 28,723,723 (GRCm39) |
K670E |
possibly damaging |
Het |
H2bc7 |
G |
A |
13: 23,758,277 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
G |
T |
1: 150,579,924 (GRCm39) |
Q1938K |
possibly damaging |
Het |
Hnrnpk |
T |
C |
13: 58,546,971 (GRCm39) |
D71G |
probably damaging |
Het |
Hspa4l |
G |
A |
3: 40,722,411 (GRCm39) |
R311H |
probably damaging |
Het |
Igkv3-5 |
T |
A |
6: 70,640,688 (GRCm39) |
F56L |
probably benign |
Het |
Igkv6-20 |
T |
A |
6: 70,312,898 (GRCm39) |
T92S |
possibly damaging |
Het |
Krt8 |
C |
T |
15: 101,909,029 (GRCm39) |
V200I |
possibly damaging |
Het |
Lamb2 |
A |
T |
9: 108,357,587 (GRCm39) |
T66S |
possibly damaging |
Het |
Lamp3 |
A |
G |
16: 19,519,778 (GRCm39) |
L135S |
probably benign |
Het |
Lrguk |
A |
G |
6: 34,106,078 (GRCm39) |
Y701C |
probably damaging |
Het |
Mcc |
G |
T |
18: 44,582,388 (GRCm39) |
L588M |
probably damaging |
Het |
Mcidas |
T |
A |
13: 113,135,120 (GRCm39) |
L234Q |
probably damaging |
Het |
Mtmr14 |
T |
A |
6: 113,257,575 (GRCm39) |
L208Q |
probably damaging |
Het |
Myof |
A |
G |
19: 37,893,747 (GRCm39) |
F1139L |
possibly damaging |
Het |
Nlrp14 |
C |
A |
7: 106,781,703 (GRCm39) |
T300K |
probably benign |
Het |
Or2d36 |
A |
T |
7: 106,746,535 (GRCm39) |
E4V |
possibly damaging |
Het |
Or2m13 |
T |
A |
16: 19,226,694 (GRCm39) |
H24L |
probably benign |
Het |
Or5b118 |
A |
G |
19: 13,448,870 (GRCm39) |
I179V |
probably benign |
Het |
Or8b41 |
A |
T |
9: 38,055,097 (GRCm39) |
Y217F |
probably damaging |
Het |
Orc2 |
A |
G |
1: 58,511,547 (GRCm39) |
I354T |
probably damaging |
Het |
Pard3b |
G |
T |
1: 62,115,568 (GRCm39) |
S140I |
probably damaging |
Het |
Pcgf5 |
A |
G |
19: 36,412,003 (GRCm39) |
D49G |
probably benign |
Het |
Pcsk6 |
T |
C |
7: 65,609,041 (GRCm39) |
F388S |
probably damaging |
Het |
Prokr2 |
A |
C |
2: 132,223,362 (GRCm39) |
I60S |
probably damaging |
Het |
Rab33b |
A |
G |
3: 51,391,900 (GRCm39) |
T50A |
possibly damaging |
Het |
Rbms3 |
T |
C |
9: 116,548,457 (GRCm39) |
D61G |
probably damaging |
Het |
Rhcg |
T |
A |
7: 79,250,262 (GRCm39) |
K274* |
probably null |
Het |
Rnf112 |
C |
T |
11: 61,341,848 (GRCm39) |
V319M |
possibly damaging |
Het |
Rnf44 |
A |
T |
13: 54,830,613 (GRCm39) |
S265T |
possibly damaging |
Het |
Sf3a3 |
A |
G |
4: 124,615,851 (GRCm39) |
D168G |
probably damaging |
Het |
Sik2 |
A |
G |
9: 50,806,642 (GRCm39) |
|
probably null |
Het |
Slco1a5 |
T |
A |
6: 142,198,839 (GRCm39) |
L275F |
probably benign |
Het |
Smtnl1 |
T |
C |
2: 84,645,722 (GRCm39) |
H383R |
probably damaging |
Het |
Spns3 |
T |
G |
11: 72,429,904 (GRCm39) |
T175P |
probably damaging |
Het |
Togaram1 |
A |
G |
12: 65,042,312 (GRCm39) |
T1174A |
probably benign |
Het |
Tradd |
C |
T |
8: 105,987,277 (GRCm39) |
E10K |
possibly damaging |
Het |
Ttc7b |
A |
T |
12: 100,339,819 (GRCm39) |
Y579N |
probably damaging |
Het |
Uncx |
G |
A |
5: 139,533,344 (GRCm39) |
G470R |
probably damaging |
Het |
Vav3 |
T |
A |
3: 109,408,777 (GRCm39) |
M177K |
probably damaging |
Het |
Wfs1 |
A |
T |
5: 37,125,094 (GRCm39) |
I599N |
probably damaging |
Het |
Zfp454 |
G |
A |
11: 50,764,449 (GRCm39) |
H217Y |
probably damaging |
Het |
|
Other mutations in Akap6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Akap6
|
APN |
12 |
53,187,763 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00505:Akap6
|
APN |
12 |
52,933,885 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01134:Akap6
|
APN |
12 |
52,984,000 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01458:Akap6
|
APN |
12 |
52,933,601 (GRCm39) |
nonsense |
probably null |
|
IGL01589:Akap6
|
APN |
12 |
53,186,447 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01592:Akap6
|
APN |
12 |
53,188,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01738:Akap6
|
APN |
12 |
52,933,600 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01867:Akap6
|
APN |
12 |
52,934,791 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02025:Akap6
|
APN |
12 |
53,187,118 (GRCm39) |
missense |
probably benign |
|
IGL02041:Akap6
|
APN |
12 |
53,187,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02058:Akap6
|
APN |
12 |
53,187,338 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02194:Akap6
|
APN |
12 |
52,933,606 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02226:Akap6
|
APN |
12 |
53,057,250 (GRCm39) |
splice site |
probably benign |
|
IGL02323:Akap6
|
APN |
12 |
53,187,212 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02449:Akap6
|
APN |
12 |
53,186,971 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02475:Akap6
|
APN |
12 |
53,186,277 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02546:Akap6
|
APN |
12 |
52,927,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02547:Akap6
|
APN |
12 |
53,187,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02588:Akap6
|
APN |
12 |
52,933,282 (GRCm39) |
nonsense |
probably null |
|
IGL02608:Akap6
|
APN |
12 |
53,057,389 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02884:Akap6
|
APN |
12 |
52,933,405 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02945:Akap6
|
APN |
12 |
52,927,620 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03029:Akap6
|
APN |
12 |
52,933,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03129:Akap6
|
APN |
12 |
53,187,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Akap6
|
UTSW |
12 |
53,186,254 (GRCm39) |
nonsense |
probably null |
|
R0166:Akap6
|
UTSW |
12 |
53,187,707 (GRCm39) |
missense |
probably benign |
0.04 |
R0189:Akap6
|
UTSW |
12 |
53,188,037 (GRCm39) |
missense |
probably benign |
0.41 |
R0532:Akap6
|
UTSW |
12 |
52,934,766 (GRCm39) |
missense |
probably benign |
0.00 |
R0632:Akap6
|
UTSW |
12 |
52,983,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R0666:Akap6
|
UTSW |
12 |
52,958,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Akap6
|
UTSW |
12 |
53,188,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R0763:Akap6
|
UTSW |
12 |
53,188,997 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0785:Akap6
|
UTSW |
12 |
52,933,405 (GRCm39) |
missense |
probably benign |
0.00 |
R0879:Akap6
|
UTSW |
12 |
52,927,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0880:Akap6
|
UTSW |
12 |
53,186,291 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1033:Akap6
|
UTSW |
12 |
53,116,005 (GRCm39) |
missense |
probably damaging |
0.97 |
R1055:Akap6
|
UTSW |
12 |
52,927,455 (GRCm39) |
nonsense |
probably null |
|
R1199:Akap6
|
UTSW |
12 |
52,842,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Akap6
|
UTSW |
12 |
52,933,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R1389:Akap6
|
UTSW |
12 |
53,186,303 (GRCm39) |
missense |
probably benign |
0.15 |
R1471:Akap6
|
UTSW |
12 |
53,188,279 (GRCm39) |
missense |
probably benign |
0.05 |
R1483:Akap6
|
UTSW |
12 |
52,842,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Akap6
|
UTSW |
12 |
52,983,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1648:Akap6
|
UTSW |
12 |
53,188,789 (GRCm39) |
nonsense |
probably null |
|
R1791:Akap6
|
UTSW |
12 |
53,115,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Akap6
|
UTSW |
12 |
53,188,958 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1888:Akap6
|
UTSW |
12 |
53,188,958 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1891:Akap6
|
UTSW |
12 |
53,188,958 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1899:Akap6
|
UTSW |
12 |
53,188,635 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1917:Akap6
|
UTSW |
12 |
53,151,395 (GRCm39) |
missense |
probably benign |
0.13 |
R1970:Akap6
|
UTSW |
12 |
52,985,258 (GRCm39) |
missense |
probably damaging |
0.96 |
R1987:Akap6
|
UTSW |
12 |
53,187,578 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1988:Akap6
|
UTSW |
12 |
53,187,578 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2153:Akap6
|
UTSW |
12 |
53,188,187 (GRCm39) |
missense |
probably benign |
0.03 |
R2567:Akap6
|
UTSW |
12 |
52,985,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R2568:Akap6
|
UTSW |
12 |
52,934,061 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3025:Akap6
|
UTSW |
12 |
53,186,926 (GRCm39) |
missense |
probably benign |
|
R3051:Akap6
|
UTSW |
12 |
52,933,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R3195:Akap6
|
UTSW |
12 |
53,119,240 (GRCm39) |
nonsense |
probably null |
|
R3196:Akap6
|
UTSW |
12 |
53,119,240 (GRCm39) |
nonsense |
probably null |
|
R3426:Akap6
|
UTSW |
12 |
52,934,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R3783:Akap6
|
UTSW |
12 |
52,927,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R3934:Akap6
|
UTSW |
12 |
53,187,227 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3936:Akap6
|
UTSW |
12 |
53,187,227 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3967:Akap6
|
UTSW |
12 |
53,188,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R3970:Akap6
|
UTSW |
12 |
53,188,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R4042:Akap6
|
UTSW |
12 |
53,186,162 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4095:Akap6
|
UTSW |
12 |
53,186,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R4152:Akap6
|
UTSW |
12 |
53,187,190 (GRCm39) |
missense |
probably benign |
0.45 |
R4231:Akap6
|
UTSW |
12 |
53,187,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R4232:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4233:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4234:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4235:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4236:Akap6
|
UTSW |
12 |
53,186,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4475:Akap6
|
UTSW |
12 |
53,188,426 (GRCm39) |
missense |
probably benign |
0.00 |
R4513:Akap6
|
UTSW |
12 |
52,842,787 (GRCm39) |
missense |
probably benign |
0.03 |
R4686:Akap6
|
UTSW |
12 |
52,934,406 (GRCm39) |
frame shift |
probably null |
|
R4724:Akap6
|
UTSW |
12 |
52,842,668 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4782:Akap6
|
UTSW |
12 |
52,934,406 (GRCm39) |
frame shift |
probably null |
|
R4852:Akap6
|
UTSW |
12 |
53,151,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R5024:Akap6
|
UTSW |
12 |
53,189,345 (GRCm39) |
missense |
probably benign |
0.01 |
R5116:Akap6
|
UTSW |
12 |
53,188,298 (GRCm39) |
missense |
probably benign |
0.01 |
R5164:Akap6
|
UTSW |
12 |
53,189,249 (GRCm39) |
missense |
probably benign |
|
R5225:Akap6
|
UTSW |
12 |
52,933,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R5269:Akap6
|
UTSW |
12 |
53,186,626 (GRCm39) |
missense |
probably damaging |
0.99 |
R5352:Akap6
|
UTSW |
12 |
52,842,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R5496:Akap6
|
UTSW |
12 |
53,187,436 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5551:Akap6
|
UTSW |
12 |
52,842,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R6137:Akap6
|
UTSW |
12 |
53,187,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Akap6
|
UTSW |
12 |
53,072,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Akap6
|
UTSW |
12 |
53,189,141 (GRCm39) |
missense |
probably benign |
|
R6307:Akap6
|
UTSW |
12 |
53,188,351 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6351:Akap6
|
UTSW |
12 |
53,188,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R6479:Akap6
|
UTSW |
12 |
53,187,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R6502:Akap6
|
UTSW |
12 |
53,186,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R6760:Akap6
|
UTSW |
12 |
53,186,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6778:Akap6
|
UTSW |
12 |
53,072,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R6837:Akap6
|
UTSW |
12 |
53,188,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R6896:Akap6
|
UTSW |
12 |
52,934,277 (GRCm39) |
missense |
probably benign |
0.06 |
R6917:Akap6
|
UTSW |
12 |
53,115,951 (GRCm39) |
missense |
probably null |
0.97 |
R6983:Akap6
|
UTSW |
12 |
52,934,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R7142:Akap6
|
UTSW |
12 |
52,934,147 (GRCm39) |
missense |
probably benign |
0.02 |
R7143:Akap6
|
UTSW |
12 |
52,934,147 (GRCm39) |
missense |
probably benign |
0.02 |
R7216:Akap6
|
UTSW |
12 |
53,187,240 (GRCm39) |
missense |
probably benign |
0.02 |
R7297:Akap6
|
UTSW |
12 |
52,934,147 (GRCm39) |
missense |
probably benign |
0.02 |
R7356:Akap6
|
UTSW |
12 |
52,958,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Akap6
|
UTSW |
12 |
53,189,357 (GRCm39) |
missense |
probably benign |
0.00 |
R7382:Akap6
|
UTSW |
12 |
53,188,954 (GRCm39) |
missense |
probably benign |
0.00 |
R7498:Akap6
|
UTSW |
12 |
53,189,488 (GRCm39) |
nonsense |
probably null |
|
R7542:Akap6
|
UTSW |
12 |
53,116,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R7589:Akap6
|
UTSW |
12 |
53,188,846 (GRCm39) |
nonsense |
probably null |
|
R7676:Akap6
|
UTSW |
12 |
52,933,633 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7814:Akap6
|
UTSW |
12 |
53,187,744 (GRCm39) |
missense |
probably benign |
0.28 |
R7971:Akap6
|
UTSW |
12 |
53,186,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R8039:Akap6
|
UTSW |
12 |
53,188,459 (GRCm39) |
missense |
probably benign |
0.00 |
R8425:Akap6
|
UTSW |
12 |
52,933,404 (GRCm39) |
missense |
probably benign |
0.00 |
R8747:Akap6
|
UTSW |
12 |
53,188,999 (GRCm39) |
missense |
probably benign |
0.01 |
R8885:Akap6
|
UTSW |
12 |
53,188,319 (GRCm39) |
missense |
probably benign |
|
R8956:Akap6
|
UTSW |
12 |
53,187,127 (GRCm39) |
missense |
probably benign |
0.00 |
R8989:Akap6
|
UTSW |
12 |
52,927,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R9014:Akap6
|
UTSW |
12 |
53,186,403 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9031:Akap6
|
UTSW |
12 |
53,188,831 (GRCm39) |
missense |
probably benign |
0.36 |
R9216:Akap6
|
UTSW |
12 |
52,927,668 (GRCm39) |
missense |
probably benign |
0.05 |
R9220:Akap6
|
UTSW |
12 |
53,187,232 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9243:Akap6
|
UTSW |
12 |
53,188,035 (GRCm39) |
missense |
probably benign |
0.08 |
R9286:Akap6
|
UTSW |
12 |
53,119,254 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9347:Akap6
|
UTSW |
12 |
53,115,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R9475:Akap6
|
UTSW |
12 |
53,057,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R9509:Akap6
|
UTSW |
12 |
53,189,021 (GRCm39) |
missense |
probably damaging |
0.99 |
R9523:Akap6
|
UTSW |
12 |
52,842,672 (GRCm39) |
missense |
probably benign |
0.02 |
R9600:Akap6
|
UTSW |
12 |
52,933,341 (GRCm39) |
missense |
probably benign |
0.04 |
R9612:Akap6
|
UTSW |
12 |
52,958,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Akap6
|
UTSW |
12 |
53,151,413 (GRCm39) |
missense |
|
|
R9666:Akap6
|
UTSW |
12 |
53,188,318 (GRCm39) |
missense |
probably benign |
|
R9784:Akap6
|
UTSW |
12 |
53,187,853 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Akap6
|
UTSW |
12 |
53,189,144 (GRCm39) |
missense |
probably benign |
0.43 |
Z1176:Akap6
|
UTSW |
12 |
53,187,227 (GRCm39) |
missense |
possibly damaging |
0.92 |
|