Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700028K03Rik |
A |
G |
5: 107,687,057 (GRCm39) |
T15A |
possibly damaging |
Het |
2010315B03Rik |
G |
T |
9: 124,056,652 (GRCm39) |
Q91K |
|
Het |
2210408I21Rik |
A |
G |
13: 77,407,988 (GRCm39) |
N419S |
possibly damaging |
Het |
Abhd2 |
A |
G |
7: 78,998,020 (GRCm39) |
E184G |
probably damaging |
Het |
Adgrg3 |
T |
C |
8: 95,766,186 (GRCm39) |
I339T |
probably benign |
Het |
Adgrv1 |
C |
T |
13: 81,567,178 (GRCm39) |
A5332T |
|
Het |
Akap13 |
T |
C |
7: 75,293,193 (GRCm39) |
V42A |
|
Het |
Apob |
A |
T |
12: 8,052,069 (GRCm39) |
D1170V |
probably damaging |
Het |
Atad1 |
A |
G |
19: 32,684,323 (GRCm39) |
I25T |
possibly damaging |
Het |
Atp4b |
G |
T |
8: 13,436,746 (GRCm39) |
N255K |
probably damaging |
Het |
Atr |
C |
T |
9: 95,792,610 (GRCm39) |
A1644V |
possibly damaging |
Het |
Bpnt1 |
T |
A |
1: 185,077,584 (GRCm39) |
C100S |
probably damaging |
Het |
C1rl |
C |
T |
6: 124,484,054 (GRCm39) |
L203F |
probably benign |
Het |
Clasp2 |
T |
A |
9: 113,705,372 (GRCm39) |
V576D |
probably damaging |
Het |
Col8a2 |
A |
G |
4: 126,205,273 (GRCm39) |
T428A |
unknown |
Het |
Copg2 |
T |
A |
6: 30,749,505 (GRCm39) |
|
probably null |
Het |
Cpn2 |
C |
T |
16: 30,078,759 (GRCm39) |
R314H |
possibly damaging |
Het |
Cpt2 |
G |
A |
4: 107,764,354 (GRCm39) |
A470V |
probably damaging |
Het |
Cyp2a4 |
C |
T |
7: 26,011,688 (GRCm39) |
T303I |
probably damaging |
Het |
Ddx42 |
A |
G |
11: 106,132,606 (GRCm39) |
D543G |
probably benign |
Het |
Dip2a |
T |
C |
10: 76,112,438 (GRCm39) |
T1087A |
probably damaging |
Het |
Fam219b |
T |
C |
9: 57,444,919 (GRCm39) |
F6L |
probably benign |
Het |
Fsip2 |
G |
T |
2: 82,807,972 (GRCm39) |
L1430F |
probably damaging |
Het |
Fstl4 |
A |
G |
11: 53,075,466 (GRCm39) |
I573V |
probably benign |
Het |
Ggnbp2 |
A |
T |
11: 84,745,188 (GRCm39) |
S182R |
probably benign |
Het |
Glud1 |
A |
G |
14: 34,061,931 (GRCm39) |
T484A |
probably benign |
Het |
Gm19410 |
A |
G |
8: 36,257,608 (GRCm39) |
N682S |
probably benign |
Het |
Gnao1 |
T |
C |
8: 94,622,861 (GRCm39) |
I55T |
|
Het |
H2bc15 |
G |
T |
13: 21,938,305 (GRCm39) |
A5S |
unknown |
Het |
Hcn4 |
C |
T |
9: 58,766,809 (GRCm39) |
S790L |
unknown |
Het |
Ighv3-4 |
T |
C |
12: 114,217,393 (GRCm39) |
E66G |
probably damaging |
Het |
Igkv6-23 |
A |
G |
6: 70,237,526 (GRCm39) |
S72P |
probably damaging |
Het |
Kdm7a |
A |
C |
6: 39,147,767 (GRCm39) |
Y213D |
probably damaging |
Het |
Klk15 |
T |
G |
7: 43,587,770 (GRCm39) |
M66R |
possibly damaging |
Het |
Lce1d |
T |
A |
3: 92,593,363 (GRCm39) |
T17S |
unknown |
Het |
Lipt1 |
T |
C |
1: 37,914,534 (GRCm39) |
Y197H |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,660,978 (GRCm39) |
D157E |
|
Het |
Ltbp1 |
A |
G |
17: 75,697,498 (GRCm39) |
T1697A |
probably benign |
Het |
Marchf6 |
T |
C |
15: 31,498,845 (GRCm39) |
T151A |
probably benign |
Het |
Muc5b |
G |
A |
7: 141,396,116 (GRCm39) |
R124H |
unknown |
Het |
Myo5b |
A |
G |
18: 74,861,968 (GRCm39) |
N1320S |
possibly damaging |
Het |
Myt1l |
T |
A |
12: 29,877,611 (GRCm39) |
S421T |
unknown |
Het |
Nav1 |
A |
T |
1: 135,379,929 (GRCm39) |
M1531K |
unknown |
Het |
Nlrp4e |
A |
G |
7: 23,054,636 (GRCm39) |
D930G |
probably benign |
Het |
Nup210l |
C |
T |
3: 90,107,173 (GRCm39) |
P1570L |
probably benign |
Het |
Or51a6 |
A |
G |
7: 102,604,464 (GRCm39) |
S115P |
probably damaging |
Het |
Or5b112 |
G |
T |
19: 13,319,848 (GRCm39) |
C242F |
probably damaging |
Het |
Or5b120 |
A |
T |
19: 13,479,712 (GRCm39) |
M2L |
probably benign |
Het |
Or5d47 |
A |
T |
2: 87,804,945 (GRCm39) |
Y21* |
probably null |
Het |
Or6k14 |
A |
T |
1: 173,927,608 (GRCm39) |
I195F |
probably damaging |
Het |
Or7g30 |
G |
A |
9: 19,352,580 (GRCm39) |
V124I |
possibly damaging |
Het |
Oxct2b |
A |
T |
4: 123,011,483 (GRCm39) |
I468F |
probably damaging |
Het |
Pcdhgb7 |
T |
A |
18: 37,886,636 (GRCm39) |
L602Q |
probably damaging |
Het |
Prrc2c |
A |
G |
1: 162,525,298 (GRCm39) |
V1862A |
unknown |
Het |
Rad54l2 |
C |
T |
9: 106,573,151 (GRCm39) |
R1110H |
probably damaging |
Het |
Rere |
T |
A |
4: 150,703,636 (GRCm39) |
H180Q |
probably damaging |
Het |
Rtl1 |
C |
T |
12: 109,561,113 (GRCm39) |
R242Q |
unknown |
Het |
Sfxn4 |
T |
C |
19: 60,845,807 (GRCm39) |
D63G |
probably damaging |
Het |
Strn |
C |
T |
17: 78,967,575 (GRCm39) |
A579T |
probably benign |
Het |
Stxbp3 |
A |
G |
3: 108,747,756 (GRCm39) |
L10P |
probably damaging |
Het |
Swi5 |
T |
C |
2: 32,170,739 (GRCm39) |
M95V |
possibly damaging |
Het |
Tln2 |
T |
C |
9: 67,165,766 (GRCm39) |
Y1027C |
probably damaging |
Het |
Tmem65 |
A |
G |
15: 58,662,002 (GRCm39) |
|
probably null |
Het |
Tox4 |
C |
T |
14: 52,529,166 (GRCm39) |
P376S |
probably benign |
Het |
Tsg101 |
C |
T |
7: 46,542,308 (GRCm39) |
G215D |
possibly damaging |
Het |
Utp18 |
A |
G |
11: 93,768,833 (GRCm39) |
S226P |
probably damaging |
Het |
Vipr2 |
T |
C |
12: 116,093,788 (GRCm39) |
S174P |
probably damaging |
Het |
Vmn2r24 |
G |
T |
6: 123,763,950 (GRCm39) |
V276F |
possibly damaging |
Het |
Wdr26 |
T |
C |
1: 181,013,620 (GRCm39) |
R418G |
probably benign |
Het |
Zfp235 |
T |
C |
7: 23,840,381 (GRCm39) |
Y267H |
probably benign |
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 |
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 |
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 |
|