Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
C |
T |
9: 124,056,529 (GRCm39) |
E132K |
|
Het |
Acss2 |
T |
C |
2: 155,397,877 (GRCm39) |
I313T |
possibly damaging |
Het |
Ankrd27 |
T |
C |
7: 35,316,306 (GRCm39) |
V524A |
probably benign |
Het |
Cacna1e |
T |
C |
1: 154,341,568 (GRCm39) |
I1209V |
probably benign |
Het |
Cntn3 |
A |
T |
6: 102,414,860 (GRCm39) |
I29N |
possibly damaging |
Het |
Col5a1 |
G |
A |
2: 27,870,533 (GRCm39) |
|
probably benign |
Het |
Cttnbp2 |
G |
C |
6: 18,426,092 (GRCm39) |
A762G |
possibly damaging |
Het |
Edc3 |
C |
A |
9: 57,620,659 (GRCm39) |
|
probably benign |
Het |
Egflam |
A |
T |
15: 7,276,525 (GRCm39) |
M547K |
possibly damaging |
Het |
Fgr |
T |
C |
4: 132,725,790 (GRCm39) |
Y400H |
probably damaging |
Het |
Gaa |
C |
T |
11: 119,163,762 (GRCm39) |
P205S |
probably benign |
Het |
Gpr6 |
T |
A |
10: 40,946,911 (GRCm39) |
T224S |
probably benign |
Het |
Hes3 |
T |
C |
4: 152,371,938 (GRCm39) |
|
probably benign |
Het |
Hydin |
T |
C |
8: 111,310,541 (GRCm39) |
F4079S |
probably damaging |
Het |
Igf2bp2 |
A |
T |
16: 21,894,849 (GRCm39) |
I366N |
probably damaging |
Het |
Kmt2c |
A |
G |
5: 25,556,232 (GRCm39) |
V1171A |
probably damaging |
Het |
Kndc1 |
T |
A |
7: 139,490,536 (GRCm39) |
F346Y |
possibly damaging |
Het |
Lpin2 |
G |
A |
17: 71,537,370 (GRCm39) |
G306R |
probably benign |
Het |
Mok |
T |
C |
12: 110,781,351 (GRCm39) |
|
probably benign |
Het |
Nolc1 |
T |
C |
19: 46,070,023 (GRCm39) |
V265A |
unknown |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
Or2ah1 |
T |
G |
2: 85,653,957 (GRCm39) |
L214R |
possibly damaging |
Het |
Or4c103 |
G |
A |
2: 88,513,537 (GRCm39) |
Q180* |
probably null |
Het |
Or5j1 |
A |
C |
2: 86,879,190 (GRCm39) |
L130R |
probably damaging |
Het |
Or6b2b |
A |
G |
1: 92,418,997 (GRCm39) |
V160A |
possibly damaging |
Het |
Parp14 |
G |
A |
16: 35,677,004 (GRCm39) |
T988I |
probably benign |
Het |
Pdk1 |
A |
T |
2: 71,705,796 (GRCm39) |
Q81H |
probably benign |
Het |
Plekha6 |
A |
G |
1: 133,191,544 (GRCm39) |
T38A |
probably benign |
Het |
Pou2f1 |
A |
G |
1: 165,722,472 (GRCm39) |
|
probably null |
Het |
Rgs6 |
A |
G |
12: 83,163,066 (GRCm39) |
D424G |
probably null |
Het |
Rnf13 |
T |
G |
3: 57,714,491 (GRCm39) |
Y183* |
probably null |
Het |
Ryr2 |
A |
T |
13: 11,603,026 (GRCm39) |
|
probably null |
Het |
Serpinb7 |
T |
A |
1: 107,362,487 (GRCm39) |
S64T |
possibly damaging |
Het |
Six2 |
T |
C |
17: 85,995,100 (GRCm39) |
E94G |
probably damaging |
Het |
Slc44a5 |
A |
G |
3: 153,953,447 (GRCm39) |
I276M |
possibly damaging |
Het |
Smco2 |
A |
G |
6: 146,769,633 (GRCm39) |
Y239C |
probably damaging |
Het |
Ssx2ip |
T |
C |
3: 146,128,666 (GRCm39) |
S148P |
probably damaging |
Het |
Tiam2 |
T |
C |
17: 3,498,671 (GRCm39) |
Y816H |
possibly damaging |
Het |
Tnk2 |
C |
T |
16: 32,487,183 (GRCm39) |
R127C |
probably benign |
Het |
Tpd52l1 |
T |
C |
10: 31,208,913 (GRCm39) |
N185S |
probably benign |
Het |
Try5 |
T |
C |
6: 41,290,421 (GRCm39) |
D21G |
probably benign |
Het |
Vmn2r20 |
A |
G |
6: 123,373,369 (GRCm39) |
V491A |
possibly damaging |
Het |
Vps54 |
G |
T |
11: 21,225,095 (GRCm39) |
R197L |
probably damaging |
Het |
Xkr5 |
G |
T |
8: 18,998,736 (GRCm39) |
Y27* |
probably null |
Het |
Zfp1004 |
A |
G |
2: 150,034,266 (GRCm39) |
S196G |
possibly damaging |
Het |
Zfp626 |
T |
A |
7: 27,518,140 (GRCm39) |
C374S |
possibly 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 |
R4962:Akap13
|
UTSW |
7 |
75,399,178 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
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 |
|