Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
T |
A |
7: 45,630,481 (GRCm39) |
I1260F |
probably damaging |
Het |
Acat2 |
A |
G |
17: 13,162,774 (GRCm39) |
V358A |
probably benign |
Het |
Adgrv1 |
G |
A |
13: 81,636,081 (GRCm39) |
A3476V |
possibly damaging |
Het |
Asb2 |
G |
T |
12: 103,311,943 (GRCm39) |
Q60K |
probably benign |
Het |
Asxl3 |
A |
T |
18: 22,650,134 (GRCm39) |
R708* |
probably null |
Het |
Cd79b |
C |
T |
11: 106,203,539 (GRCm39) |
G116D |
probably damaging |
Het |
Copg2 |
A |
G |
6: 30,835,757 (GRCm39) |
F218S |
probably benign |
Het |
Defa5 |
A |
C |
8: 21,787,604 (GRCm39) |
E50D |
possibly damaging |
Het |
Efcab3 |
T |
A |
11: 104,890,107 (GRCm39) |
|
probably null |
Het |
Eva1c |
T |
A |
16: 90,663,236 (GRCm39) |
V91D |
probably damaging |
Het |
Fosb |
T |
C |
7: 19,043,283 (GRCm39) |
Y25C |
probably damaging |
Het |
Gm5141 |
G |
A |
13: 62,922,201 (GRCm39) |
H323Y |
probably damaging |
Het |
Gpr19 |
T |
C |
6: 134,847,398 (GRCm39) |
N58S |
probably benign |
Het |
Gpr26 |
G |
A |
7: 131,585,893 (GRCm39) |
A288T |
possibly damaging |
Het |
Gucy2g |
T |
A |
19: 55,229,460 (GRCm39) |
Q70L |
probably damaging |
Het |
Ifit2 |
C |
T |
19: 34,550,897 (GRCm39) |
R146* |
probably null |
Het |
Lgr5 |
A |
C |
10: 115,293,772 (GRCm39) |
N408K |
possibly damaging |
Het |
Lrp1 |
G |
A |
10: 127,396,005 (GRCm39) |
H2422Y |
probably damaging |
Het |
Mief1 |
T |
A |
15: 80,132,692 (GRCm39) |
Y191* |
probably null |
Het |
Npr3 |
C |
G |
15: 11,905,518 (GRCm39) |
A70P |
probably damaging |
Het |
Or2y1b |
A |
T |
11: 49,208,541 (GRCm39) |
H56L |
probably damaging |
Het |
Pcnt |
A |
G |
10: 76,265,032 (GRCm39) |
|
probably null |
Het |
Pnlip |
A |
T |
19: 58,660,174 (GRCm39) |
D29V |
probably benign |
Het |
Pnpt1 |
T |
A |
11: 29,088,567 (GRCm39) |
F277I |
possibly damaging |
Het |
Pou2f2 |
A |
C |
7: 24,793,006 (GRCm39) |
V441G |
probably damaging |
Het |
Prdm4 |
A |
G |
10: 85,740,002 (GRCm39) |
V459A |
probably benign |
Het |
Ptprs |
A |
T |
17: 56,729,195 (GRCm39) |
V855E |
probably damaging |
Het |
Rflna |
A |
G |
5: 125,088,352 (GRCm39) |
T100A |
probably benign |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Spata31h1 |
A |
T |
10: 82,131,871 (GRCm39) |
S380T |
probably benign |
Het |
Syn3 |
A |
G |
10: 85,893,428 (GRCm39) |
S472P |
unknown |
Het |
Taar8a |
A |
T |
10: 23,952,674 (GRCm39) |
I93F |
possibly damaging |
Het |
Taok2 |
T |
A |
7: 126,477,930 (GRCm39) |
D207V |
probably damaging |
Het |
Tpst2 |
A |
T |
5: 112,424,600 (GRCm39) |
|
probably benign |
Homo |
Trdv2-1 |
A |
G |
14: 54,183,999 (GRCm39) |
N77S |
possibly damaging |
Het |
Wdr17 |
A |
C |
8: 55,134,559 (GRCm39) |
V18G |
probably benign |
Het |
Zbtb17 |
T |
C |
4: 141,192,261 (GRCm39) |
V402A |
probably damaging |
Het |
Zfp772 |
T |
C |
7: 7,208,547 (GRCm39) |
E99G |
possibly damaging |
Het |
Zw10 |
A |
G |
9: 48,980,926 (GRCm39) |
D442G |
probably benign |
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 |
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 |
|