Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
T |
19: 9,015,251 (GRCm38) |
D4633V |
probably damaging |
Het |
Arhgef28 |
T |
C |
13: 97,967,096 (GRCm38) |
M803V |
probably benign |
Het |
Bltp1 |
T |
A |
3: 36,953,985 (GRCm38) |
|
probably null |
Het |
Bltp2 |
A |
T |
11: 78,268,167 (GRCm38) |
Q433L |
probably damaging |
Het |
Ccdc73 |
T |
A |
2: 104,931,045 (GRCm38) |
L130* |
probably null |
Het |
Ccdc73 |
A |
G |
2: 104,999,159 (GRCm38) |
E1059G |
probably damaging |
Het |
Ccer2 |
A |
C |
7: 28,757,283 (GRCm38) |
S151R |
possibly damaging |
Het |
Cep128 |
T |
A |
12: 91,230,829 (GRCm38) |
H406L |
probably benign |
Het |
Cep135 |
A |
G |
5: 76,597,428 (GRCm38) |
D229G |
probably benign |
Het |
Cpvl |
T |
A |
6: 53,954,611 (GRCm38) |
D103V |
probably benign |
Het |
Crppa |
T |
A |
12: 36,521,996 (GRCm38) |
L301Q |
probably damaging |
Het |
Cstdc6 |
C |
A |
16: 36,321,832 (GRCm38) |
G61C |
probably damaging |
Het |
Disp3 |
G |
A |
4: 148,258,753 (GRCm38) |
A567V |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,343,591 (GRCm38) |
I2379T |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,095,044 (GRCm38) |
Y2433C |
probably damaging |
Het |
Dock3 |
A |
G |
9: 107,108,421 (GRCm38) |
I85T |
probably benign |
Het |
Dock9 |
A |
C |
14: 121,591,830 (GRCm38) |
S1380A |
probably benign |
Het |
Erbin |
T |
C |
13: 103,886,203 (GRCm38) |
T43A |
probably benign |
Het |
Fastkd3 |
T |
C |
13: 68,585,241 (GRCm38) |
V502A |
possibly damaging |
Het |
Fn1 |
T |
C |
1: 71,651,625 (GRCm38) |
H59R |
probably damaging |
Het |
Fsd2 |
A |
G |
7: 81,559,659 (GRCm38) |
V145A |
possibly damaging |
Het |
Fzr1 |
A |
G |
10: 81,370,319 (GRCm38) |
V178A |
probably damaging |
Het |
Gnpnat1 |
T |
C |
14: 45,380,998 (GRCm38) |
R116G |
probably damaging |
Het |
Grm7 |
T |
A |
6: 110,914,511 (GRCm38) |
V235E |
probably damaging |
Het |
Hdac4 |
A |
C |
1: 91,934,645 (GRCm38) |
N1002K |
probably damaging |
Het |
Hey1 |
C |
T |
3: 8,664,897 (GRCm38) |
A167T |
probably benign |
Het |
Hrnr |
A |
G |
3: 93,332,604 (GRCm38) |
N3383S |
unknown |
Het |
Ints2 |
A |
T |
11: 86,217,800 (GRCm38) |
V907D |
probably benign |
Het |
Jchain |
T |
A |
5: 88,521,467 (GRCm38) |
Q109L |
probably damaging |
Het |
Klhdc7a |
A |
T |
4: 139,966,024 (GRCm38) |
Y537* |
probably null |
Het |
Klra1 |
C |
T |
6: 130,377,779 (GRCm38) |
S92N |
probably benign |
Het |
Krt31 |
C |
T |
11: 100,049,580 (GRCm38) |
G150S |
probably benign |
Het |
Lrrc71 |
G |
A |
3: 87,742,643 (GRCm38) |
T326M |
probably benign |
Het |
Lrrn4 |
T |
C |
2: 132,870,443 (GRCm38) |
T487A |
probably benign |
Het |
Map4k5 |
T |
G |
12: 69,842,912 (GRCm38) |
R198S |
probably damaging |
Het |
Men1 |
G |
A |
19: 6,338,837 (GRCm38) |
C354Y |
probably damaging |
Het |
Ms4a18 |
A |
T |
19: 11,013,655 (GRCm38) |
V25E |
probably damaging |
Het |
Mutyh |
T |
A |
4: 116,819,368 (GRCm38) |
S512R |
possibly damaging |
Het |
Myh10 |
G |
T |
11: 68,814,496 (GRCm38) |
A1947S |
possibly damaging |
Het |
Nfasc |
T |
C |
1: 132,610,886 (GRCm38) |
D427G |
probably damaging |
Het |
Nlrp9c |
A |
G |
7: 26,378,056 (GRCm38) |
M767T |
probably benign |
Het |
Nrbp1 |
T |
C |
5: 31,245,391 (GRCm38) |
L185P |
probably damaging |
Het |
Pcdh9 |
G |
A |
14: 93,888,305 (GRCm38) |
P143L |
probably damaging |
Het |
Pcsk6 |
A |
T |
7: 65,927,287 (GRCm38) |
M158L |
possibly damaging |
Het |
Pkd1 |
G |
T |
17: 24,576,592 (GRCm38) |
|
probably null |
Het |
Plk4 |
A |
T |
3: 40,805,817 (GRCm38) |
S383C |
possibly damaging |
Het |
Plxna2 |
T |
C |
1: 194,643,989 (GRCm38) |
L77P |
probably damaging |
Het |
Pnpla6 |
A |
T |
8: 3,542,370 (GRCm38) |
T1209S |
probably benign |
Het |
Prdm2 |
A |
G |
4: 143,132,509 (GRCm38) |
S1404P |
possibly damaging |
Het |
Preb |
T |
C |
5: 30,958,813 (GRCm38) |
D150G |
probably damaging |
Het |
Prrt2 |
A |
G |
7: 127,018,730 (GRCm38) |
V59A |
probably benign |
Het |
Prss40 |
T |
C |
1: 34,558,014 (GRCm38) |
N151S |
possibly damaging |
Het |
Ptprt |
A |
G |
2: 161,766,321 (GRCm38) |
V685A |
possibly damaging |
Het |
Ptprt |
G |
T |
2: 161,558,898 (GRCm38) |
A1053D |
probably damaging |
Het |
Rfx4 |
C |
T |
10: 84,896,088 (GRCm38) |
S549F |
possibly damaging |
Het |
Rnaset2b |
T |
A |
17: 6,996,477 (GRCm38) |
V87E |
probably benign |
Het |
Rnf213 |
G |
A |
11: 119,441,107 (GRCm38) |
E2381K |
probably damaging |
Het |
Sectm1a |
A |
T |
11: 121,069,680 (GRCm38) |
I103N |
probably damaging |
Het |
Selp |
T |
A |
1: 164,142,758 (GRCm38) |
L597Q |
probably damaging |
Het |
Sema6a |
T |
C |
18: 47,300,142 (GRCm38) |
D74G |
probably damaging |
Het |
Serpinb9b |
T |
C |
13: 33,029,559 (GRCm38) |
V33A |
probably benign |
Het |
Setd1b |
A |
T |
5: 123,147,706 (GRCm38) |
T272S |
unknown |
Het |
Sgf29 |
G |
C |
7: 126,649,477 (GRCm38) |
|
probably null |
Het |
Slc4a10 |
C |
A |
2: 62,268,204 (GRCm38) |
Q561K |
probably damaging |
Het |
Slc4a5 |
T |
C |
6: 83,273,232 (GRCm38) |
I649T |
possibly damaging |
Het |
Slc5a7 |
A |
G |
17: 54,293,835 (GRCm38) |
Y91H |
probably damaging |
Het |
Styxl1 |
T |
C |
5: 135,757,122 (GRCm38) |
Y23C |
probably damaging |
Het |
Tbc1d24 |
A |
G |
17: 24,206,872 (GRCm38) |
V490A |
possibly damaging |
Het |
Tbpl2 |
A |
T |
2: 24,094,732 (GRCm38) |
F133L |
probably benign |
Het |
Tnfrsf22 |
T |
C |
7: 143,638,389 (GRCm38) |
|
probably benign |
Het |
Top2b |
A |
G |
14: 16,398,916 (GRCm38) |
E512G |
probably damaging |
Het |
Trgc3 |
C |
A |
13: 19,260,994 (GRCm38) |
F37L |
probably damaging |
Het |
Ttc17 |
T |
A |
2: 94,364,345 (GRCm38) |
H561L |
probably benign |
Het |
Ttll4 |
G |
T |
1: 74,685,368 (GRCm38) |
V566L |
possibly damaging |
Het |
Ubqlnl |
A |
G |
7: 104,148,485 (GRCm38) |
Y602H |
probably benign |
Het |
Vmn1r231 |
T |
A |
17: 20,889,950 (GRCm38) |
E234D |
probably damaging |
Het |
Wbp11 |
A |
G |
6: 136,820,585 (GRCm38) |
S279P |
probably damaging |
Het |
Wdr6 |
A |
G |
9: 108,576,534 (GRCm38) |
L50P |
probably damaging |
Het |
Zfp715 |
A |
C |
7: 43,298,649 (GRCm38) |
I629S |
possibly damaging |
Het |
|
Other mutations in Akap6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Akap6
|
APN |
12 |
53,140,980 (GRCm38) |
missense |
possibly damaging |
0.79 |
IGL00505:Akap6
|
APN |
12 |
52,887,102 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL01134:Akap6
|
APN |
12 |
52,937,217 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01458:Akap6
|
APN |
12 |
52,886,818 (GRCm38) |
nonsense |
probably null |
|
IGL01589:Akap6
|
APN |
12 |
53,139,664 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01592:Akap6
|
APN |
12 |
53,142,142 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01738:Akap6
|
APN |
12 |
52,886,817 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01867:Akap6
|
APN |
12 |
52,888,008 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02025:Akap6
|
APN |
12 |
53,140,335 (GRCm38) |
missense |
probably benign |
|
IGL02041:Akap6
|
APN |
12 |
53,140,653 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02058:Akap6
|
APN |
12 |
53,140,555 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02194:Akap6
|
APN |
12 |
52,886,823 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02226:Akap6
|
APN |
12 |
53,010,467 (GRCm38) |
splice site |
probably benign |
|
IGL02323:Akap6
|
APN |
12 |
53,140,429 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02449:Akap6
|
APN |
12 |
53,140,188 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02475:Akap6
|
APN |
12 |
53,139,494 (GRCm38) |
missense |
probably benign |
0.03 |
IGL02546:Akap6
|
APN |
12 |
52,880,738 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02547:Akap6
|
APN |
12 |
53,140,696 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02588:Akap6
|
APN |
12 |
52,886,499 (GRCm38) |
nonsense |
probably null |
|
IGL02608:Akap6
|
APN |
12 |
53,010,606 (GRCm38) |
missense |
probably benign |
0.39 |
IGL02884:Akap6
|
APN |
12 |
52,886,622 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02945:Akap6
|
APN |
12 |
52,880,837 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03029:Akap6
|
APN |
12 |
52,886,412 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03129:Akap6
|
APN |
12 |
53,140,306 (GRCm38) |
missense |
probably damaging |
1.00 |
R0133:Akap6
|
UTSW |
12 |
53,139,471 (GRCm38) |
nonsense |
probably null |
|
R0166:Akap6
|
UTSW |
12 |
53,140,924 (GRCm38) |
missense |
probably benign |
0.04 |
R0189:Akap6
|
UTSW |
12 |
53,141,254 (GRCm38) |
missense |
probably benign |
0.41 |
R0532:Akap6
|
UTSW |
12 |
52,887,983 (GRCm38) |
missense |
probably benign |
0.00 |
R0632:Akap6
|
UTSW |
12 |
52,937,148 (GRCm38) |
missense |
probably damaging |
1.00 |
R0666:Akap6
|
UTSW |
12 |
52,911,808 (GRCm38) |
missense |
probably damaging |
1.00 |
R0723:Akap6
|
UTSW |
12 |
53,141,902 (GRCm38) |
missense |
probably damaging |
1.00 |
R0763:Akap6
|
UTSW |
12 |
53,142,214 (GRCm38) |
missense |
possibly damaging |
0.93 |
R0785:Akap6
|
UTSW |
12 |
52,886,622 (GRCm38) |
missense |
probably benign |
0.00 |
R0879:Akap6
|
UTSW |
12 |
52,880,799 (GRCm38) |
missense |
probably damaging |
1.00 |
R0880:Akap6
|
UTSW |
12 |
53,139,508 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1033:Akap6
|
UTSW |
12 |
53,069,222 (GRCm38) |
missense |
probably damaging |
0.97 |
R1055:Akap6
|
UTSW |
12 |
52,880,672 (GRCm38) |
nonsense |
probably null |
|
R1199:Akap6
|
UTSW |
12 |
52,796,190 (GRCm38) |
missense |
probably damaging |
1.00 |
R1295:Akap6
|
UTSW |
12 |
52,887,029 (GRCm38) |
missense |
probably damaging |
1.00 |
R1389:Akap6
|
UTSW |
12 |
53,139,520 (GRCm38) |
missense |
probably benign |
0.15 |
R1471:Akap6
|
UTSW |
12 |
53,141,496 (GRCm38) |
missense |
probably benign |
0.05 |
R1483:Akap6
|
UTSW |
12 |
52,796,087 (GRCm38) |
missense |
probably damaging |
1.00 |
R1512:Akap6
|
UTSW |
12 |
52,937,154 (GRCm38) |
missense |
probably damaging |
1.00 |
R1648:Akap6
|
UTSW |
12 |
53,142,006 (GRCm38) |
nonsense |
probably null |
|
R1791:Akap6
|
UTSW |
12 |
53,069,125 (GRCm38) |
missense |
probably damaging |
1.00 |
R1888:Akap6
|
UTSW |
12 |
53,142,175 (GRCm38) |
missense |
possibly damaging |
0.88 |
R1888:Akap6
|
UTSW |
12 |
53,142,175 (GRCm38) |
missense |
possibly damaging |
0.88 |
R1891:Akap6
|
UTSW |
12 |
53,142,175 (GRCm38) |
missense |
possibly damaging |
0.88 |
R1899:Akap6
|
UTSW |
12 |
53,141,852 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1917:Akap6
|
UTSW |
12 |
53,104,612 (GRCm38) |
missense |
probably benign |
0.13 |
R1970:Akap6
|
UTSW |
12 |
52,938,475 (GRCm38) |
missense |
probably damaging |
0.96 |
R1988:Akap6
|
UTSW |
12 |
53,140,795 (GRCm38) |
missense |
possibly damaging |
0.78 |
R2153:Akap6
|
UTSW |
12 |
53,141,404 (GRCm38) |
missense |
probably benign |
0.03 |
R2567:Akap6
|
UTSW |
12 |
52,938,373 (GRCm38) |
missense |
probably damaging |
1.00 |
R2568:Akap6
|
UTSW |
12 |
52,887,278 (GRCm38) |
missense |
possibly damaging |
0.77 |
R3025:Akap6
|
UTSW |
12 |
53,140,143 (GRCm38) |
missense |
probably benign |
|
R3051:Akap6
|
UTSW |
12 |
52,887,033 (GRCm38) |
missense |
probably damaging |
1.00 |
R3195:Akap6
|
UTSW |
12 |
53,072,457 (GRCm38) |
nonsense |
probably null |
|
R3196:Akap6
|
UTSW |
12 |
53,072,457 (GRCm38) |
nonsense |
probably null |
|
R3426:Akap6
|
UTSW |
12 |
52,888,034 (GRCm38) |
missense |
probably damaging |
1.00 |
R3783:Akap6
|
UTSW |
12 |
52,880,769 (GRCm38) |
missense |
probably damaging |
1.00 |
R3934:Akap6
|
UTSW |
12 |
53,140,444 (GRCm38) |
missense |
possibly damaging |
0.92 |
R3936:Akap6
|
UTSW |
12 |
53,140,444 (GRCm38) |
missense |
possibly damaging |
0.92 |
R3967:Akap6
|
UTSW |
12 |
53,141,453 (GRCm38) |
missense |
probably damaging |
1.00 |
R3970:Akap6
|
UTSW |
12 |
53,141,453 (GRCm38) |
missense |
probably damaging |
1.00 |
R4042:Akap6
|
UTSW |
12 |
53,139,379 (GRCm38) |
critical splice acceptor site |
probably null |
|
R4095:Akap6
|
UTSW |
12 |
53,139,462 (GRCm38) |
missense |
probably damaging |
1.00 |
R4152:Akap6
|
UTSW |
12 |
53,140,407 (GRCm38) |
missense |
probably benign |
0.45 |
R4231:Akap6
|
UTSW |
12 |
53,141,038 (GRCm38) |
missense |
probably damaging |
1.00 |
R4232:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4233:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4234:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4235:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4236:Akap6
|
UTSW |
12 |
53,139,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R4475:Akap6
|
UTSW |
12 |
53,141,643 (GRCm38) |
missense |
probably benign |
0.00 |
R4513:Akap6
|
UTSW |
12 |
52,796,004 (GRCm38) |
missense |
probably benign |
0.03 |
R4686:Akap6
|
UTSW |
12 |
52,887,623 (GRCm38) |
frame shift |
probably null |
|
R4724:Akap6
|
UTSW |
12 |
52,795,885 (GRCm38) |
missense |
possibly damaging |
0.80 |
R4782:Akap6
|
UTSW |
12 |
52,887,623 (GRCm38) |
frame shift |
probably null |
|
R4852:Akap6
|
UTSW |
12 |
53,104,675 (GRCm38) |
missense |
probably damaging |
1.00 |
R5024:Akap6
|
UTSW |
12 |
53,142,562 (GRCm38) |
missense |
probably benign |
0.01 |
R5116:Akap6
|
UTSW |
12 |
53,141,515 (GRCm38) |
missense |
probably benign |
0.01 |
R5164:Akap6
|
UTSW |
12 |
53,142,466 (GRCm38) |
missense |
probably benign |
|
R5225:Akap6
|
UTSW |
12 |
52,886,546 (GRCm38) |
missense |
probably damaging |
1.00 |
R5269:Akap6
|
UTSW |
12 |
53,139,843 (GRCm38) |
missense |
probably damaging |
0.99 |
R5352:Akap6
|
UTSW |
12 |
52,796,097 (GRCm38) |
missense |
probably damaging |
1.00 |
R5496:Akap6
|
UTSW |
12 |
53,140,653 (GRCm38) |
missense |
possibly damaging |
0.87 |
R5551:Akap6
|
UTSW |
12 |
52,795,964 (GRCm38) |
missense |
probably damaging |
1.00 |
R5997:Akap6
|
UTSW |
12 |
52,937,233 (GRCm38) |
critical splice donor site |
probably null |
|
R6137:Akap6
|
UTSW |
12 |
53,140,354 (GRCm38) |
missense |
probably damaging |
1.00 |
R6151:Akap6
|
UTSW |
12 |
53,025,792 (GRCm38) |
missense |
probably damaging |
1.00 |
R6169:Akap6
|
UTSW |
12 |
53,142,358 (GRCm38) |
missense |
probably benign |
|
R6307:Akap6
|
UTSW |
12 |
53,141,568 (GRCm38) |
missense |
possibly damaging |
0.85 |
R6351:Akap6
|
UTSW |
12 |
53,142,025 (GRCm38) |
missense |
probably damaging |
0.98 |
R6479:Akap6
|
UTSW |
12 |
53,141,169 (GRCm38) |
missense |
probably damaging |
1.00 |
R6502:Akap6
|
UTSW |
12 |
53,140,215 (GRCm38) |
missense |
probably damaging |
1.00 |
R6760:Akap6
|
UTSW |
12 |
53,139,778 (GRCm38) |
missense |
probably damaging |
1.00 |
R6778:Akap6
|
UTSW |
12 |
53,025,816 (GRCm38) |
missense |
probably damaging |
1.00 |
R6837:Akap6
|
UTSW |
12 |
53,141,262 (GRCm38) |
missense |
probably damaging |
1.00 |
R6896:Akap6
|
UTSW |
12 |
52,887,494 (GRCm38) |
missense |
probably benign |
0.06 |
R6917:Akap6
|
UTSW |
12 |
53,069,168 (GRCm38) |
missense |
probably null |
0.97 |
R6983:Akap6
|
UTSW |
12 |
52,887,653 (GRCm38) |
missense |
probably damaging |
1.00 |
R7142:Akap6
|
UTSW |
12 |
52,887,364 (GRCm38) |
missense |
probably benign |
0.02 |
R7143:Akap6
|
UTSW |
12 |
52,887,364 (GRCm38) |
missense |
probably benign |
0.02 |
R7216:Akap6
|
UTSW |
12 |
53,140,457 (GRCm38) |
missense |
probably benign |
0.02 |
R7297:Akap6
|
UTSW |
12 |
52,887,364 (GRCm38) |
missense |
probably benign |
0.02 |
R7356:Akap6
|
UTSW |
12 |
52,911,864 (GRCm38) |
missense |
probably damaging |
1.00 |
R7378:Akap6
|
UTSW |
12 |
53,142,574 (GRCm38) |
missense |
probably benign |
0.00 |
R7382:Akap6
|
UTSW |
12 |
53,142,171 (GRCm38) |
missense |
probably benign |
0.00 |
R7498:Akap6
|
UTSW |
12 |
53,142,705 (GRCm38) |
nonsense |
probably null |
|
R7542:Akap6
|
UTSW |
12 |
53,069,234 (GRCm38) |
missense |
probably damaging |
1.00 |
R7589:Akap6
|
UTSW |
12 |
53,142,063 (GRCm38) |
nonsense |
probably null |
|
R7676:Akap6
|
UTSW |
12 |
52,886,850 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7814:Akap6
|
UTSW |
12 |
53,140,961 (GRCm38) |
missense |
probably benign |
0.28 |
R7971:Akap6
|
UTSW |
12 |
53,139,795 (GRCm38) |
missense |
probably damaging |
1.00 |
R8039:Akap6
|
UTSW |
12 |
53,141,676 (GRCm38) |
missense |
probably benign |
0.00 |
R8425:Akap6
|
UTSW |
12 |
52,886,621 (GRCm38) |
missense |
probably benign |
0.00 |
R8747:Akap6
|
UTSW |
12 |
53,142,216 (GRCm38) |
missense |
probably benign |
0.01 |
R8885:Akap6
|
UTSW |
12 |
53,141,536 (GRCm38) |
missense |
probably benign |
|
R8956:Akap6
|
UTSW |
12 |
53,140,344 (GRCm38) |
missense |
probably benign |
0.00 |
R8989:Akap6
|
UTSW |
12 |
52,880,871 (GRCm38) |
missense |
probably damaging |
1.00 |
R9014:Akap6
|
UTSW |
12 |
53,139,620 (GRCm38) |
missense |
possibly damaging |
0.60 |
R9031:Akap6
|
UTSW |
12 |
53,142,048 (GRCm38) |
missense |
probably benign |
0.36 |
R9216:Akap6
|
UTSW |
12 |
52,880,885 (GRCm38) |
missense |
probably benign |
0.05 |
R9220:Akap6
|
UTSW |
12 |
53,140,449 (GRCm38) |
missense |
possibly damaging |
0.49 |
R9243:Akap6
|
UTSW |
12 |
53,141,252 (GRCm38) |
missense |
probably benign |
0.08 |
R9286:Akap6
|
UTSW |
12 |
53,072,471 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9347:Akap6
|
UTSW |
12 |
53,069,111 (GRCm38) |
missense |
probably damaging |
1.00 |
R9475:Akap6
|
UTSW |
12 |
53,010,552 (GRCm38) |
missense |
probably damaging |
1.00 |
R9509:Akap6
|
UTSW |
12 |
53,142,238 (GRCm38) |
missense |
probably damaging |
0.99 |
R9523:Akap6
|
UTSW |
12 |
52,795,889 (GRCm38) |
missense |
probably benign |
0.02 |
R9600:Akap6
|
UTSW |
12 |
52,886,558 (GRCm38) |
missense |
probably benign |
0.04 |
R9612:Akap6
|
UTSW |
12 |
52,911,907 (GRCm38) |
missense |
probably damaging |
1.00 |
R9627:Akap6
|
UTSW |
12 |
53,104,630 (GRCm38) |
missense |
|
|
R9666:Akap6
|
UTSW |
12 |
53,141,535 (GRCm38) |
missense |
probably benign |
|
R9784:Akap6
|
UTSW |
12 |
53,141,070 (GRCm38) |
missense |
probably damaging |
1.00 |
X0062:Akap6
|
UTSW |
12 |
53,142,361 (GRCm38) |
missense |
probably benign |
0.43 |
Z1176:Akap6
|
UTSW |
12 |
53,140,444 (GRCm38) |
missense |
possibly damaging |
0.92 |
|