Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930567H17Rik |
C |
T |
X: 69,438,135 (GRCm39) |
A53T |
probably benign |
Het |
Ajuba |
T |
C |
14: 54,806,983 (GRCm39) |
R490G |
probably damaging |
Het |
Aldh5a1 |
C |
T |
13: 25,095,636 (GRCm39) |
G494R |
probably damaging |
Het |
Ankar |
T |
C |
1: 72,697,701 (GRCm39) |
D1034G |
probably benign |
Het |
Aox3 |
T |
A |
1: 58,154,044 (GRCm39) |
N23K |
probably benign |
Het |
Arhgef18 |
T |
C |
8: 3,500,317 (GRCm39) |
I541T |
possibly damaging |
Het |
Atg14 |
T |
C |
14: 47,788,802 (GRCm39) |
K184E |
probably benign |
Het |
Bltp1 |
C |
T |
3: 36,974,385 (GRCm39) |
T663I |
probably benign |
Het |
Cacnb2 |
A |
G |
2: 14,986,251 (GRCm39) |
K343E |
probably damaging |
Het |
Casp8 |
T |
C |
1: 58,883,929 (GRCm39) |
V432A |
probably damaging |
Het |
Cd93 |
A |
T |
2: 148,284,880 (GRCm39) |
H155Q |
probably benign |
Het |
Cox6b2 |
T |
C |
7: 4,755,834 (GRCm39) |
M1V |
probably null |
Het |
Crat |
T |
C |
2: 30,303,023 (GRCm39) |
E88G |
possibly damaging |
Het |
Ddx1 |
C |
T |
12: 13,273,858 (GRCm39) |
V590I |
possibly damaging |
Het |
Dip2a |
G |
A |
10: 76,155,304 (GRCm39) |
P94S |
probably damaging |
Het |
Dtx3 |
A |
G |
10: 127,029,058 (GRCm39) |
I60T |
possibly damaging |
Het |
Filip1l |
T |
C |
16: 57,327,131 (GRCm39) |
S54P |
probably benign |
Het |
Gm12887 |
A |
T |
4: 121,479,299 (GRCm39) |
M1K |
probably null |
Het |
Gm26678 |
T |
C |
3: 54,540,504 (GRCm39) |
|
noncoding transcript |
Het |
Impg1 |
A |
G |
9: 80,252,611 (GRCm39) |
L523P |
probably damaging |
Het |
Insyn2b |
A |
T |
11: 34,353,143 (GRCm39) |
E395V |
probably benign |
Het |
Ip6k2 |
G |
A |
9: 108,682,847 (GRCm39) |
R319Q |
probably benign |
Het |
Irak2 |
A |
G |
6: 113,667,817 (GRCm39) |
E466G |
probably damaging |
Het |
Irgm2 |
C |
T |
11: 58,110,304 (GRCm39) |
|
probably benign |
Het |
Jak3 |
T |
A |
8: 72,138,189 (GRCm39) |
V880D |
probably damaging |
Het |
Jmy |
G |
T |
13: 93,635,433 (GRCm39) |
P128T |
probably benign |
Het |
Kif20a |
A |
G |
18: 34,765,091 (GRCm39) |
N775S |
probably benign |
Het |
Kremen1 |
G |
A |
11: 5,193,881 (GRCm39) |
Q50* |
probably null |
Het |
Lrrc71 |
A |
G |
3: 87,648,298 (GRCm39) |
I438T |
probably benign |
Het |
Map3k1 |
T |
C |
13: 111,905,028 (GRCm39) |
T374A |
probably benign |
Het |
Med12l |
T |
G |
3: 59,164,644 (GRCm39) |
|
probably null |
Het |
Mrps30 |
T |
C |
13: 118,523,376 (GRCm39) |
D132G |
probably damaging |
Het |
Mta1 |
T |
C |
12: 113,099,447 (GRCm39) |
M603T |
possibly damaging |
Het |
Myo5a |
A |
G |
9: 75,097,279 (GRCm39) |
N1319S |
possibly damaging |
Het |
Nalcn |
T |
A |
14: 123,837,325 (GRCm39) |
Q13L |
probably benign |
Het |
Nbas |
A |
G |
12: 13,443,344 (GRCm39) |
N1133S |
probably damaging |
Het |
Nsun2 |
A |
G |
13: 69,767,660 (GRCm39) |
N205D |
probably damaging |
Het |
Nxpe4 |
A |
T |
9: 48,310,137 (GRCm39) |
T467S |
probably damaging |
Het |
Or13a20 |
T |
C |
7: 140,232,653 (GRCm39) |
Y254H |
probably damaging |
Het |
Or4f17-ps1 |
C |
T |
2: 111,358,546 (GRCm39) |
R314C |
probably damaging |
Het |
Or7g30 |
T |
A |
9: 19,352,886 (GRCm39) |
L226I |
probably damaging |
Het |
Pam |
A |
G |
1: 97,811,849 (GRCm39) |
|
probably null |
Het |
Pcdh7 |
G |
A |
5: 57,876,631 (GRCm39) |
G62D |
possibly damaging |
Het |
Plxna2 |
C |
T |
1: 194,326,762 (GRCm39) |
T232I |
probably damaging |
Het |
Prkar1b |
A |
G |
5: 139,094,376 (GRCm39) |
S71P |
probably benign |
Het |
Ptprq |
A |
T |
10: 107,522,144 (GRCm39) |
Y602* |
probably null |
Het |
Rfx4 |
A |
T |
10: 84,650,558 (GRCm39) |
M84L |
probably benign |
Het |
Rfx7 |
A |
T |
9: 72,526,672 (GRCm39) |
E1287D |
possibly damaging |
Het |
Rin2 |
C |
T |
2: 145,702,366 (GRCm39) |
T354I |
probably benign |
Het |
Rnf216 |
A |
T |
5: 143,078,845 (GRCm39) |
S35T |
probably damaging |
Het |
Rps6kc1 |
A |
G |
1: 190,541,097 (GRCm39) |
V402A |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Sart3 |
A |
G |
5: 113,909,479 (GRCm39) |
M73T |
probably benign |
Het |
Scn10a |
G |
T |
9: 119,460,610 (GRCm39) |
T1088K |
probably damaging |
Het |
Senp2 |
T |
C |
16: 21,830,304 (GRCm39) |
|
probably null |
Het |
Setd7 |
T |
C |
3: 51,450,151 (GRCm39) |
N92D |
probably benign |
Het |
Sipa1 |
A |
T |
19: 5,704,117 (GRCm39) |
L735Q |
probably damaging |
Het |
Skint11 |
C |
A |
4: 114,101,856 (GRCm39) |
Q99K |
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,988,820 (GRCm39) |
S296T |
probably benign |
Het |
Spc24 |
T |
C |
9: 21,667,498 (GRCm39) |
|
probably null |
Het |
Tex15 |
T |
C |
8: 34,062,165 (GRCm39) |
S806P |
probably damaging |
Het |
Tgm3 |
A |
T |
2: 129,886,509 (GRCm39) |
K577* |
probably null |
Het |
Wscd2 |
A |
G |
5: 113,699,045 (GRCm39) |
D200G |
probably benign |
Het |
Xpo6 |
T |
C |
7: 125,773,354 (GRCm39) |
T24A |
possibly damaging |
Het |
Zfhx2 |
A |
G |
14: 55,310,991 (GRCm39) |
C568R |
possibly damaging |
Het |
Zfp599 |
T |
A |
9: 22,161,041 (GRCm39) |
K375* |
probably null |
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 |
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 |
R5997:Akap6
|
UTSW |
12 |
52,984,016 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
|