Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930455H04Rik |
C |
A |
3: 116,762,120 (GRCm39) |
|
probably benign |
Het |
Actn3 |
C |
T |
19: 4,921,798 (GRCm39) |
|
probably null |
Het |
Akap9 |
A |
T |
5: 4,094,048 (GRCm39) |
Q2190L |
possibly damaging |
Het |
Ankrd6 |
A |
T |
4: 32,823,452 (GRCm39) |
V190D |
possibly damaging |
Het |
Atrn |
T |
A |
2: 130,841,157 (GRCm39) |
D1186E |
probably benign |
Het |
Bank1 |
A |
T |
3: 135,989,934 (GRCm39) |
V52E |
probably damaging |
Het |
Blmh |
A |
G |
11: 76,857,883 (GRCm39) |
N342D |
probably benign |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Ces2f |
A |
G |
8: 105,677,669 (GRCm39) |
T225A |
probably damaging |
Het |
Clic6 |
G |
T |
16: 92,296,245 (GRCm39) |
D302Y |
probably damaging |
Het |
Clmn |
T |
A |
12: 104,763,341 (GRCm39) |
N95I |
probably damaging |
Het |
Cmya5 |
A |
T |
13: 93,232,840 (GRCm39) |
F749L |
probably benign |
Het |
Cramp1 |
A |
G |
17: 25,202,956 (GRCm39) |
F358L |
probably damaging |
Het |
Dhx38 |
T |
C |
8: 110,283,098 (GRCm39) |
D573G |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,584,471 (GRCm39) |
Y625H |
probably damaging |
Het |
Enpep |
A |
G |
3: 129,115,007 (GRCm39) |
|
probably null |
Het |
Fat1 |
T |
C |
8: 45,483,350 (GRCm39) |
L3146P |
probably damaging |
Het |
Gal3st2b |
G |
A |
1: 93,868,570 (GRCm39) |
S265N |
probably benign |
Het |
Glis3 |
G |
A |
19: 28,643,266 (GRCm39) |
A92V |
possibly damaging |
Het |
Gm266 |
T |
C |
12: 111,452,173 (GRCm39) |
D11G |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,204,427 (GRCm39) |
M1L |
probably benign |
Het |
Kcnj15 |
G |
A |
16: 95,097,548 (GRCm39) |
|
probably benign |
Het |
Krt27 |
A |
G |
11: 99,239,551 (GRCm39) |
S310P |
probably damaging |
Het |
Lama2 |
A |
T |
10: 26,862,816 (GRCm39) |
D2982E |
probably damaging |
Het |
Lrfn3 |
A |
G |
7: 30,059,451 (GRCm39) |
V258A |
probably benign |
Het |
Lrit3 |
A |
T |
3: 129,594,193 (GRCm39) |
M128K |
probably damaging |
Het |
Ltbp3 |
A |
G |
19: 5,797,512 (GRCm39) |
T417A |
probably benign |
Het |
Mettl25 |
T |
C |
10: 105,601,122 (GRCm39) |
T554A |
probably benign |
Het |
Micall1 |
A |
G |
15: 79,011,198 (GRCm39) |
S523G |
probably damaging |
Het |
Mmp21 |
G |
A |
7: 133,280,700 (GRCm39) |
A90V |
probably benign |
Het |
Mon2 |
T |
C |
10: 122,895,110 (GRCm39) |
N53S |
probably benign |
Het |
Muc15 |
T |
C |
2: 110,562,252 (GRCm39) |
|
probably null |
Het |
Myo15b |
A |
T |
11: 115,773,127 (GRCm39) |
M431L |
probably benign |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nt5c3 |
T |
C |
6: 56,861,701 (GRCm39) |
D195G |
probably damaging |
Het |
Or3a1b |
T |
A |
11: 74,012,874 (GRCm39) |
M253K |
probably benign |
Het |
Or52h1 |
A |
G |
7: 103,828,949 (GRCm39) |
L222P |
possibly damaging |
Het |
Pals1 |
T |
A |
12: 78,866,115 (GRCm39) |
D313E |
probably benign |
Het |
Pgrmc2 |
A |
G |
3: 41,037,125 (GRCm39) |
L102P |
probably damaging |
Het |
Plekha1 |
T |
G |
7: 130,502,241 (GRCm39) |
|
probably benign |
Het |
Pramel23 |
T |
C |
4: 143,423,562 (GRCm39) |
Y409C |
probably damaging |
Het |
Prss59 |
A |
T |
6: 40,902,999 (GRCm39) |
Y124* |
probably null |
Het |
Ralgapa1 |
T |
G |
12: 55,749,345 (GRCm39) |
I1233L |
probably damaging |
Het |
Rb1cc1 |
T |
A |
1: 6,333,441 (GRCm39) |
D68E |
probably benign |
Het |
Rere |
C |
A |
4: 150,699,331 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
A |
T |
11: 119,321,100 (GRCm39) |
H1185L |
possibly damaging |
Het |
Robo2 |
G |
T |
16: 73,770,150 (GRCm39) |
P529T |
probably damaging |
Het |
Robo2 |
G |
A |
16: 73,770,149 (GRCm39) |
P529L |
probably damaging |
Het |
Shprh |
A |
G |
10: 11,061,181 (GRCm39) |
T1165A |
possibly damaging |
Het |
Slc22a26 |
C |
T |
19: 7,768,390 (GRCm39) |
|
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,690,450 (GRCm39) |
L456P |
probably damaging |
Het |
Slc5a8 |
T |
C |
10: 88,740,885 (GRCm39) |
Y267H |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,068,902 (GRCm39) |
I927T |
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,362,006 (GRCm39) |
D156G |
probably benign |
Het |
Sox5 |
A |
T |
6: 143,853,169 (GRCm39) |
S370T |
probably benign |
Het |
Spen |
T |
C |
4: 141,201,374 (GRCm39) |
T2418A |
probably damaging |
Het |
St8sia6 |
A |
T |
2: 13,701,705 (GRCm39) |
L104H |
probably damaging |
Het |
Stox1 |
T |
A |
10: 62,500,430 (GRCm39) |
N710I |
probably damaging |
Het |
Syncrip |
T |
C |
9: 88,344,900 (GRCm39) |
|
probably benign |
Het |
Syt11 |
G |
A |
3: 88,655,051 (GRCm39) |
P417S |
probably damaging |
Het |
Taf2 |
A |
T |
15: 54,910,849 (GRCm39) |
N608K |
probably benign |
Het |
Tfcp2l1 |
G |
A |
1: 118,596,447 (GRCm39) |
G394E |
possibly damaging |
Het |
Tial1 |
A |
G |
7: 128,056,715 (GRCm39) |
I13T |
probably damaging |
Het |
Tmem108 |
T |
C |
9: 103,361,981 (GRCm39) |
D535G |
probably benign |
Het |
Tpp1 |
T |
C |
7: 105,396,626 (GRCm39) |
M464V |
probably benign |
Het |
Trrap |
C |
A |
5: 144,757,063 (GRCm39) |
N2108K |
probably damaging |
Het |
Tspan3 |
T |
C |
9: 56,053,883 (GRCm39) |
D156G |
probably benign |
Het |
Ttn |
C |
T |
2: 76,592,607 (GRCm39) |
V20842I |
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,190,886 (GRCm39) |
W4078R |
probably damaging |
Het |
Uts2r |
G |
A |
11: 121,051,795 (GRCm39) |
V220M |
possibly damaging |
Het |
Vmn2r19 |
G |
A |
6: 123,293,283 (GRCm39) |
|
probably null |
Het |
Vmn2r3 |
A |
T |
3: 64,166,673 (GRCm39) |
F819L |
probably damaging |
Het |
Wdtc1 |
T |
C |
4: 133,031,470 (GRCm39) |
Y250C |
probably damaging |
Het |
Zan |
T |
C |
5: 137,393,888 (GRCm39) |
H4521R |
unknown |
Het |
Zfp219 |
A |
T |
14: 52,244,224 (GRCm39) |
C652S |
probably 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 |
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 |
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 |
|