Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
A |
T |
3: 138,173,582 (GRCm38) |
L235Q |
probably damaging |
Het |
Aadacl4fm4 |
A |
T |
4: 144,686,220 (GRCm38) |
M50K |
possibly damaging |
Het |
Adam6b |
T |
A |
12: 113,490,655 (GRCm38) |
V364D |
probably benign |
Het |
Anapc11 |
T |
C |
11: 120,605,377 (GRCm38) |
V69A |
probably benign |
Het |
Ankmy1 |
C |
T |
1: 92,896,190 (GRCm38) |
R118Q |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,638,053 (GRCm38) |
S931P |
probably benign |
Het |
Atp6v1c2 |
G |
A |
12: 17,288,168 (GRCm38) |
R280C |
probably damaging |
Het |
Bbs10 |
T |
A |
10: 111,300,052 (GRCm38) |
I342N |
probably damaging |
Het |
Calhm2 |
T |
C |
19: 47,132,950 (GRCm38) |
D260G |
possibly damaging |
Het |
Camk2a |
A |
G |
18: 60,958,238 (GRCm38) |
E264G |
probably damaging |
Het |
Ccdc146 |
T |
A |
5: 21,319,545 (GRCm38) |
M270L |
probably benign |
Het |
Cdc16 |
A |
G |
8: 13,779,264 (GRCm38) |
T517A |
probably benign |
Het |
Ces1g |
T |
C |
8: 93,331,193 (GRCm38) |
H160R |
probably benign |
Het |
Chst4 |
T |
C |
8: 110,030,394 (GRCm38) |
N196S |
probably damaging |
Het |
Ciz1 |
A |
T |
2: 32,367,467 (GRCm38) |
N175Y |
probably damaging |
Het |
Cyb5r4 |
G |
A |
9: 87,027,040 (GRCm38) |
V57I |
probably damaging |
Het |
Cyth3 |
A |
G |
5: 143,684,426 (GRCm38) |
|
probably benign |
Het |
Def6 |
A |
G |
17: 28,220,180 (GRCm38) |
E255G |
probably damaging |
Het |
Dhtkd1 |
T |
G |
2: 5,911,870 (GRCm38) |
Q665P |
probably damaging |
Het |
Dsg3 |
A |
C |
18: 20,539,747 (GRCm38) |
D825A |
probably damaging |
Het |
Eif3m |
T |
C |
2: 105,005,000 (GRCm38) |
T242A |
probably benign |
Het |
Emilin3 |
A |
G |
2: 160,909,817 (GRCm38) |
F101L |
probably benign |
Het |
Epha7 |
A |
G |
4: 28,935,700 (GRCm38) |
|
probably null |
Het |
Fbxo45 |
A |
T |
16: 32,238,405 (GRCm38) |
Y224N |
probably damaging |
Het |
Fhod3 |
A |
T |
18: 25,090,104 (GRCm38) |
M836L |
possibly damaging |
Het |
Fut4 |
C |
A |
9: 14,751,210 (GRCm38) |
V263F |
probably damaging |
Het |
Ggt1 |
C |
T |
10: 75,579,270 (GRCm38) |
T206M |
probably benign |
Het |
Gls |
T |
C |
1: 52,188,699 (GRCm38) |
R79G |
probably damaging |
Het |
Grhl1 |
T |
C |
12: 24,581,515 (GRCm38) |
S156P |
probably benign |
Het |
Ipo8 |
C |
T |
6: 148,775,042 (GRCm38) |
S983N |
probably benign |
Het |
Kcna7 |
C |
T |
7: 45,409,444 (GRCm38) |
A385V |
probably damaging |
Het |
Kpnb1 |
A |
T |
11: 97,185,090 (GRCm38) |
L40Q |
probably damaging |
Het |
Matn1 |
A |
T |
4: 130,950,106 (GRCm38) |
S209C |
probably damaging |
Het |
Mcc |
A |
G |
18: 44,475,222 (GRCm38) |
I501T |
probably benign |
Het |
Mdp1 |
A |
T |
14: 55,659,375 (GRCm38) |
F104L |
probably damaging |
Het |
Mib2 |
A |
T |
4: 155,656,288 (GRCm38) |
N626K |
probably damaging |
Het |
Mrgprh |
T |
C |
17: 12,876,956 (GRCm38) |
S28P |
possibly damaging |
Het |
Mup-ps23 |
T |
A |
4: 61,856,149 (GRCm38) |
|
noncoding transcript |
Het |
Myh15 |
A |
G |
16: 49,182,959 (GRCm38) |
T1794A |
possibly damaging |
Het |
Myo18a |
C |
G |
11: 77,821,042 (GRCm38) |
P680A |
probably benign |
Het |
Myom2 |
G |
T |
8: 15,098,419 (GRCm38) |
D532Y |
possibly damaging |
Het |
Ndufaf5 |
A |
G |
2: 140,170,881 (GRCm38) |
N57S |
probably benign |
Het |
Nectin3 |
C |
T |
16: 46,458,187 (GRCm38) |
V282M |
probably damaging |
Het |
Nup188 |
G |
T |
2: 30,330,988 (GRCm38) |
D997Y |
probably damaging |
Het |
Olfm3 |
T |
C |
3: 115,122,805 (GRCm38) |
V462A |
probably damaging |
Het |
Opcml |
A |
G |
9: 28,813,398 (GRCm38) |
H164R |
possibly damaging |
Het |
Or14a259 |
A |
T |
7: 86,363,805 (GRCm38) |
C177* |
probably null |
Het |
Or4c120 |
A |
T |
2: 89,170,413 (GRCm38) |
F266L |
probably benign |
Het |
Or8u9 |
A |
C |
2: 86,171,706 (GRCm38) |
F37C |
probably damaging |
Het |
Pacrg |
A |
G |
17: 10,403,418 (GRCm38) |
I209T |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,661,215 (GRCm38) |
M522V |
probably benign |
Het |
Pck1 |
T |
A |
2: 173,153,390 (GRCm38) |
M1K |
probably null |
Het |
Pcm1 |
G |
T |
8: 41,276,111 (GRCm38) |
E707* |
probably null |
Het |
Pcsk5 |
G |
A |
19: 17,654,849 (GRCm38) |
R318W |
probably damaging |
Het |
Phf11d |
A |
T |
14: 59,353,344 (GRCm38) |
M188K |
possibly damaging |
Het |
Ppip5k2 |
A |
T |
1: 97,740,537 (GRCm38) |
C615* |
probably null |
Het |
Prkdc |
T |
A |
16: 15,791,927 (GRCm38) |
S3132T |
probably damaging |
Het |
Prl2c5 |
A |
T |
13: 13,183,024 (GRCm38) |
|
probably benign |
Het |
Prpsap2 |
A |
G |
11: 61,741,000 (GRCm38) |
I177T |
possibly damaging |
Het |
Rad50 |
A |
G |
11: 53,650,519 (GRCm38) |
S1297P |
probably damaging |
Het |
Rasip1 |
T |
A |
7: 45,635,244 (GRCm38) |
N678K |
possibly damaging |
Het |
Rubcn |
A |
G |
16: 32,835,980 (GRCm38) |
S544P |
probably damaging |
Het |
Rwdd2a |
A |
T |
9: 86,574,400 (GRCm38) |
T210S |
possibly damaging |
Het |
Scd2 |
A |
G |
19: 44,303,040 (GRCm38) |
D306G |
probably damaging |
Het |
Sema3b |
T |
C |
9: 107,602,918 (GRCm38) |
N207S |
probably benign |
Het |
Sf3b2 |
C |
T |
19: 5,274,824 (GRCm38) |
D845N |
probably damaging |
Het |
Sipa1l2 |
C |
A |
8: 125,464,410 (GRCm38) |
C947F |
probably damaging |
Het |
Slc12a1 |
A |
T |
2: 125,226,031 (GRCm38) |
T1013S |
probably damaging |
Het |
Slc18a2 |
A |
T |
19: 59,287,367 (GRCm38) |
I461L |
probably benign |
Het |
Slc1a6 |
C |
A |
10: 78,801,922 (GRCm38) |
Y427* |
probably null |
Het |
Slc30a4 |
A |
T |
2: 122,689,399 (GRCm38) |
I231K |
probably damaging |
Het |
Sos1 |
G |
T |
17: 80,453,763 (GRCm38) |
A168D |
probably damaging |
Het |
Spata31f1a |
T |
C |
4: 42,851,161 (GRCm38) |
I332V |
probably benign |
Het |
Sptb |
T |
C |
12: 76,621,371 (GRCm38) |
S651G |
probably benign |
Het |
Stk36 |
T |
C |
1: 74,633,620 (GRCm38) |
L1007P |
probably damaging |
Het |
Tek |
A |
T |
4: 94,804,341 (GRCm38) |
N229Y |
probably damaging |
Het |
Tep1 |
A |
G |
14: 50,836,768 (GRCm38) |
F1887L |
possibly damaging |
Het |
Tet1 |
A |
T |
10: 62,878,209 (GRCm38) |
C602* |
probably null |
Het |
Tnfrsf19 |
A |
G |
14: 60,972,036 (GRCm38) |
S262P |
possibly damaging |
Het |
Trim5 |
T |
C |
7: 104,265,684 (GRCm38) |
I393V |
probably benign |
Het |
Trpm6 |
A |
G |
19: 18,853,587 (GRCm38) |
E1272G |
probably benign |
Het |
Ttc21b |
A |
T |
2: 66,188,326 (GRCm38) |
Y1246N |
probably damaging |
Het |
Ttll3 |
T |
A |
6: 113,398,777 (GRCm38) |
L151H |
probably damaging |
Het |
U2surp |
C |
T |
9: 95,484,443 (GRCm38) |
V470I |
probably benign |
Het |
Ubr1 |
A |
T |
2: 120,946,657 (GRCm38) |
Y276N |
probably benign |
Het |
Uggt1 |
A |
G |
1: 36,179,670 (GRCm38) |
S59P |
probably benign |
Het |
Unc45a |
T |
C |
7: 80,326,344 (GRCm38) |
T796A |
probably damaging |
Het |
Unc5b |
C |
A |
10: 60,778,940 (GRCm38) |
V193F |
possibly damaging |
Het |
Upp1 |
G |
T |
11: 9,129,590 (GRCm38) |
M50I |
probably benign |
Het |
Vps18 |
C |
T |
2: 119,293,905 (GRCm38) |
R438C |
probably damaging |
Het |
Zfp715 |
T |
C |
7: 43,299,336 (GRCm38) |
Y400C |
possibly damaging |
Het |
Zfp955b |
T |
C |
17: 33,302,522 (GRCm38) |
Y322H |
probably benign |
Het |
|
Other mutations in Akap13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Akap13
|
APN |
7 |
75,725,971 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL00332:Akap13
|
APN |
7 |
75,728,919 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00481:Akap13
|
APN |
7 |
75,723,895 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00590:Akap13
|
APN |
7 |
75,610,669 (GRCm38) |
missense |
probably benign |
0.01 |
IGL00655:Akap13
|
APN |
7 |
75,704,398 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL00766:Akap13
|
APN |
7 |
75,704,512 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL00818:Akap13
|
APN |
7 |
75,609,727 (GRCm38) |
missense |
probably benign |
0.00 |
IGL00826:Akap13
|
APN |
7 |
75,677,447 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01014:Akap13
|
APN |
7 |
75,750,633 (GRCm38) |
utr 3 prime |
probably benign |
|
IGL01090:Akap13
|
APN |
7 |
75,666,531 (GRCm38) |
missense |
probably benign |
0.44 |
IGL01155:Akap13
|
APN |
7 |
75,569,936 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01326:Akap13
|
APN |
7 |
75,725,348 (GRCm38) |
missense |
probably benign |
0.30 |
IGL01456:Akap13
|
APN |
7 |
75,602,847 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01460:Akap13
|
APN |
7 |
75,747,846 (GRCm38) |
missense |
probably benign |
0.29 |
IGL01568:Akap13
|
APN |
7 |
75,608,522 (GRCm38) |
nonsense |
probably null |
0.00 |
IGL01610:Akap13
|
APN |
7 |
75,747,605 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01610:Akap13
|
APN |
7 |
75,720,180 (GRCm38) |
missense |
possibly damaging |
0.71 |
IGL01615:Akap13
|
APN |
7 |
75,697,393 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01667:Akap13
|
APN |
7 |
75,570,019 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01705:Akap13
|
APN |
7 |
75,746,767 (GRCm38) |
missense |
possibly damaging |
0.86 |
IGL02070:Akap13
|
APN |
7 |
75,666,545 (GRCm38) |
missense |
probably benign |
0.27 |
IGL02269:Akap13
|
APN |
7 |
75,602,911 (GRCm38) |
missense |
probably benign |
|
IGL02421:Akap13
|
APN |
7 |
75,717,806 (GRCm38) |
missense |
possibly damaging |
0.66 |
IGL02870:Akap13
|
APN |
7 |
75,609,188 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL02944:Akap13
|
APN |
7 |
75,608,657 (GRCm38) |
missense |
probably benign |
|
IGL03051:Akap13
|
APN |
7 |
75,610,485 (GRCm38) |
nonsense |
probably null |
|
IGL03160:Akap13
|
APN |
7 |
75,730,417 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03245:Akap13
|
APN |
7 |
75,609,752 (GRCm38) |
missense |
probably damaging |
0.99 |
R0254:Akap13
|
UTSW |
7 |
75,736,604 (GRCm38) |
splice site |
probably benign |
|
R0310:Akap13
|
UTSW |
7 |
75,614,930 (GRCm38) |
missense |
probably damaging |
0.99 |
R0373:Akap13
|
UTSW |
7 |
75,609,929 (GRCm38) |
missense |
probably benign |
0.00 |
R0408:Akap13
|
UTSW |
7 |
75,746,796 (GRCm38) |
missense |
probably damaging |
1.00 |
R0631:Akap13
|
UTSW |
7 |
75,614,996 (GRCm38) |
missense |
probably damaging |
0.99 |
R0646:Akap13
|
UTSW |
7 |
75,747,746 (GRCm38) |
missense |
probably damaging |
1.00 |
R0781:Akap13
|
UTSW |
7 |
75,611,377 (GRCm38) |
missense |
possibly damaging |
0.56 |
R0845:Akap13
|
UTSW |
7 |
75,725,380 (GRCm38) |
missense |
probably damaging |
1.00 |
R1004:Akap13
|
UTSW |
7 |
75,687,286 (GRCm38) |
missense |
probably damaging |
0.99 |
R1024:Akap13
|
UTSW |
7 |
75,677,409 (GRCm38) |
missense |
probably damaging |
1.00 |
R1110:Akap13
|
UTSW |
7 |
75,611,377 (GRCm38) |
missense |
possibly damaging |
0.56 |
R1346:Akap13
|
UTSW |
7 |
75,609,592 (GRCm38) |
missense |
possibly damaging |
0.67 |
R1349:Akap13
|
UTSW |
7 |
75,609,592 (GRCm38) |
missense |
possibly damaging |
0.67 |
R1372:Akap13
|
UTSW |
7 |
75,609,592 (GRCm38) |
missense |
possibly damaging |
0.67 |
R1387:Akap13
|
UTSW |
7 |
75,586,193 (GRCm38) |
missense |
probably damaging |
0.97 |
R1442:Akap13
|
UTSW |
7 |
75,735,778 (GRCm38) |
missense |
probably damaging |
0.99 |
R1466:Akap13
|
UTSW |
7 |
75,729,049 (GRCm38) |
missense |
possibly damaging |
0.79 |
R1466:Akap13
|
UTSW |
7 |
75,729,049 (GRCm38) |
missense |
possibly damaging |
0.79 |
R1584:Akap13
|
UTSW |
7 |
75,729,049 (GRCm38) |
missense |
possibly damaging |
0.79 |
R1696:Akap13
|
UTSW |
7 |
75,609,592 (GRCm38) |
missense |
possibly damaging |
0.67 |
R1738:Akap13
|
UTSW |
7 |
75,677,194 (GRCm38) |
missense |
probably damaging |
1.00 |
R1773:Akap13
|
UTSW |
7 |
75,683,451 (GRCm38) |
missense |
possibly damaging |
0.80 |
R1785:Akap13
|
UTSW |
7 |
75,611,434 (GRCm38) |
missense |
probably benign |
0.16 |
R1786:Akap13
|
UTSW |
7 |
75,611,434 (GRCm38) |
missense |
probably benign |
0.16 |
R1791:Akap13
|
UTSW |
7 |
75,611,035 (GRCm38) |
missense |
probably benign |
0.00 |
R1819:Akap13
|
UTSW |
7 |
75,608,705 (GRCm38) |
missense |
probably benign |
0.04 |
R1879:Akap13
|
UTSW |
7 |
75,610,727 (GRCm38) |
missense |
probably benign |
0.01 |
R1989:Akap13
|
UTSW |
7 |
75,704,516 (GRCm38) |
missense |
probably benign |
0.01 |
R2016:Akap13
|
UTSW |
7 |
75,704,531 (GRCm38) |
missense |
probably damaging |
0.99 |
R2092:Akap13
|
UTSW |
7 |
75,610,570 (GRCm38) |
missense |
probably benign |
0.05 |
R2126:Akap13
|
UTSW |
7 |
75,725,304 (GRCm38) |
missense |
possibly damaging |
0.95 |
R2131:Akap13
|
UTSW |
7 |
75,611,434 (GRCm38) |
missense |
probably benign |
0.16 |
R2132:Akap13
|
UTSW |
7 |
75,611,434 (GRCm38) |
missense |
probably benign |
0.16 |
R2133:Akap13
|
UTSW |
7 |
75,611,434 (GRCm38) |
missense |
probably benign |
0.16 |
R2251:Akap13
|
UTSW |
7 |
75,739,477 (GRCm38) |
missense |
possibly damaging |
0.50 |
R3704:Akap13
|
UTSW |
7 |
75,666,550 (GRCm38) |
missense |
probably damaging |
1.00 |
R3713:Akap13
|
UTSW |
7 |
75,586,181 (GRCm38) |
missense |
probably damaging |
0.98 |
R3731:Akap13
|
UTSW |
7 |
75,611,377 (GRCm38) |
missense |
probably benign |
0.39 |
R3765:Akap13
|
UTSW |
7 |
75,608,837 (GRCm38) |
missense |
probably benign |
0.04 |
R3788:Akap13
|
UTSW |
7 |
75,702,153 (GRCm38) |
critical splice donor site |
probably null |
|
R3793:Akap13
|
UTSW |
7 |
75,610,141 (GRCm38) |
missense |
probably benign |
0.00 |
R3970:Akap13
|
UTSW |
7 |
75,569,951 (GRCm38) |
nonsense |
probably null |
|
R4205:Akap13
|
UTSW |
7 |
75,610,919 (GRCm38) |
missense |
probably benign |
0.05 |
R4257:Akap13
|
UTSW |
7 |
75,611,285 (GRCm38) |
missense |
probably damaging |
0.98 |
R4374:Akap13
|
UTSW |
7 |
75,608,984 (GRCm38) |
missense |
probably damaging |
0.96 |
R4448:Akap13
|
UTSW |
7 |
75,742,760 (GRCm38) |
missense |
probably damaging |
1.00 |
R4450:Akap13
|
UTSW |
7 |
75,742,760 (GRCm38) |
missense |
probably damaging |
1.00 |
R4457:Akap13
|
UTSW |
7 |
75,739,465 (GRCm38) |
missense |
probably damaging |
0.99 |
R4458:Akap13
|
UTSW |
7 |
75,739,465 (GRCm38) |
missense |
probably damaging |
0.99 |
R4466:Akap13
|
UTSW |
7 |
75,602,773 (GRCm38) |
splice site |
probably null |
|
R4632:Akap13
|
UTSW |
7 |
75,666,553 (GRCm38) |
missense |
possibly damaging |
0.91 |
R4667:Akap13
|
UTSW |
7 |
75,729,094 (GRCm38) |
missense |
probably damaging |
1.00 |
R4669:Akap13
|
UTSW |
7 |
75,729,094 (GRCm38) |
missense |
probably damaging |
1.00 |
R4671:Akap13
|
UTSW |
7 |
75,579,564 (GRCm38) |
nonsense |
probably null |
|
R4821:Akap13
|
UTSW |
7 |
75,677,507 (GRCm38) |
intron |
probably benign |
|
R4868:Akap13
|
UTSW |
7 |
75,743,504 (GRCm38) |
missense |
probably damaging |
1.00 |
R4894:Akap13
|
UTSW |
7 |
75,725,320 (GRCm38) |
missense |
possibly damaging |
0.76 |
R4943:Akap13
|
UTSW |
7 |
75,749,240 (GRCm38) |
missense |
probably benign |
0.22 |
R4962:Akap13
|
UTSW |
7 |
75,749,430 (GRCm38) |
missense |
probably damaging |
0.98 |
R4988:Akap13
|
UTSW |
7 |
75,730,528 (GRCm38) |
missense |
probably damaging |
1.00 |
R5119:Akap13
|
UTSW |
7 |
75,687,252 (GRCm38) |
missense |
probably damaging |
0.98 |
R5141:Akap13
|
UTSW |
7 |
75,609,614 (GRCm38) |
missense |
probably benign |
0.18 |
R5419:Akap13
|
UTSW |
7 |
75,610,243 (GRCm38) |
missense |
probably benign |
0.01 |
R5427:Akap13
|
UTSW |
7 |
75,728,869 (GRCm38) |
missense |
possibly damaging |
0.89 |
R5429:Akap13
|
UTSW |
7 |
75,602,904 (GRCm38) |
missense |
possibly damaging |
0.70 |
R5432:Akap13
|
UTSW |
7 |
75,602,830 (GRCm38) |
missense |
probably damaging |
1.00 |
R5458:Akap13
|
UTSW |
7 |
75,586,301 (GRCm38) |
missense |
probably damaging |
1.00 |
R5636:Akap13
|
UTSW |
7 |
75,704,372 (GRCm38) |
missense |
probably damaging |
0.96 |
R5643:Akap13
|
UTSW |
7 |
75,702,154 (GRCm38) |
critical splice donor site |
probably null |
|
R5898:Akap13
|
UTSW |
7 |
75,729,146 (GRCm38) |
missense |
probably damaging |
1.00 |
R5932:Akap13
|
UTSW |
7 |
75,610,184 (GRCm38) |
missense |
probably damaging |
1.00 |
R6135:Akap13
|
UTSW |
7 |
75,609,908 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6137:Akap13
|
UTSW |
7 |
75,677,416 (GRCm38) |
missense |
probably damaging |
1.00 |
R6182:Akap13
|
UTSW |
7 |
75,586,280 (GRCm38) |
missense |
probably benign |
0.45 |
R6310:Akap13
|
UTSW |
7 |
75,749,193 (GRCm38) |
missense |
probably damaging |
0.99 |
R6346:Akap13
|
UTSW |
7 |
75,685,254 (GRCm38) |
missense |
probably damaging |
1.00 |
R6466:Akap13
|
UTSW |
7 |
75,727,044 (GRCm38) |
missense |
probably benign |
0.01 |
R6605:Akap13
|
UTSW |
7 |
75,579,768 (GRCm38) |
missense |
probably damaging |
0.98 |
R6617:Akap13
|
UTSW |
7 |
75,730,363 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6621:Akap13
|
UTSW |
7 |
75,569,981 (GRCm38) |
missense |
probably damaging |
1.00 |
R6703:Akap13
|
UTSW |
7 |
75,602,898 (GRCm38) |
missense |
probably damaging |
1.00 |
R6750:Akap13
|
UTSW |
7 |
75,739,458 (GRCm38) |
missense |
probably benign |
0.03 |
R7069:Akap13
|
UTSW |
7 |
75,610,262 (GRCm38) |
missense |
probably benign |
0.29 |
R7116:Akap13
|
UTSW |
7 |
75,720,195 (GRCm38) |
missense |
probably benign |
0.00 |
R7158:Akap13
|
UTSW |
7 |
75,579,594 (GRCm38) |
missense |
probably damaging |
0.97 |
R7159:Akap13
|
UTSW |
7 |
75,730,579 (GRCm38) |
missense |
possibly damaging |
0.72 |
R7467:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R7468:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R7471:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R7472:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R7477:Akap13
|
UTSW |
7 |
75,749,247 (GRCm38) |
missense |
probably benign |
|
R7636:Akap13
|
UTSW |
7 |
75,609,873 (GRCm38) |
missense |
probably benign |
0.04 |
R7650:Akap13
|
UTSW |
7 |
75,643,454 (GRCm38) |
missense |
probably benign |
0.20 |
R7671:Akap13
|
UTSW |
7 |
75,569,900 (GRCm38) |
missense |
probably damaging |
1.00 |
R7681:Akap13
|
UTSW |
7 |
75,728,796 (GRCm38) |
missense |
possibly damaging |
0.91 |
R7752:Akap13
|
UTSW |
7 |
75,677,258 (GRCm38) |
missense |
possibly damaging |
0.74 |
R7784:Akap13
|
UTSW |
7 |
75,610,328 (GRCm38) |
missense |
probably benign |
0.00 |
R7816:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R7817:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R7834:Akap13
|
UTSW |
7 |
75,742,642 (GRCm38) |
missense |
possibly damaging |
0.85 |
R7880:Akap13
|
UTSW |
7 |
75,586,216 (GRCm38) |
missense |
probably damaging |
0.97 |
R7942:Akap13
|
UTSW |
7 |
75,611,470 (GRCm38) |
missense |
possibly damaging |
0.50 |
R8006:Akap13
|
UTSW |
7 |
75,579,696 (GRCm38) |
missense |
probably damaging |
1.00 |
R8009:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R8011:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R8012:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R8013:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R8016:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R8089:Akap13
|
UTSW |
7 |
75,610,592 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8138:Akap13
|
UTSW |
7 |
75,702,231 (GRCm38) |
splice site |
probably null |
|
R8174:Akap13
|
UTSW |
7 |
75,728,869 (GRCm38) |
missense |
possibly damaging |
0.89 |
R8298:Akap13
|
UTSW |
7 |
75,747,804 (GRCm38) |
missense |
probably damaging |
1.00 |
R8444:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R8445:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R8465:Akap13
|
UTSW |
7 |
75,727,038 (GRCm38) |
missense |
probably benign |
0.11 |
R8512:Akap13
|
UTSW |
7 |
75,611,086 (GRCm38) |
missense |
probably damaging |
0.99 |
R8523:Akap13
|
UTSW |
7 |
75,730,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R8793:Akap13
|
UTSW |
7 |
75,725,328 (GRCm38) |
missense |
probably benign |
0.35 |
R8907:Akap13
|
UTSW |
7 |
75,610,708 (GRCm38) |
missense |
probably damaging |
0.99 |
R8907:Akap13
|
UTSW |
7 |
75,610,696 (GRCm38) |
missense |
probably benign |
0.08 |
R8928:Akap13
|
UTSW |
7 |
75,609,858 (GRCm38) |
missense |
probably benign |
0.00 |
R8929:Akap13
|
UTSW |
7 |
75,609,004 (GRCm38) |
missense |
probably benign |
0.00 |
R8937:Akap13
|
UTSW |
7 |
75,534,853 (GRCm38) |
critical splice donor site |
probably null |
|
R8967:Akap13
|
UTSW |
7 |
75,729,134 (GRCm38) |
missense |
possibly damaging |
0.80 |
R8986:Akap13
|
UTSW |
7 |
75,609,326 (GRCm38) |
missense |
probably benign |
|
R9152:Akap13
|
UTSW |
7 |
75,611,285 (GRCm38) |
missense |
probably damaging |
0.98 |
R9153:Akap13
|
UTSW |
7 |
75,609,481 (GRCm38) |
missense |
probably benign |
0.00 |
R9160:Akap13
|
UTSW |
7 |
75,735,778 (GRCm38) |
missense |
possibly damaging |
0.88 |
R9192:Akap13
|
UTSW |
7 |
75,704,501 (GRCm38) |
missense |
probably benign |
0.06 |
R9319:Akap13
|
UTSW |
7 |
75,609,088 (GRCm38) |
missense |
probably benign |
0.01 |
R9513:Akap13
|
UTSW |
7 |
75,704,527 (GRCm38) |
missense |
probably benign |
0.01 |
R9515:Akap13
|
UTSW |
7 |
75,704,527 (GRCm38) |
missense |
probably benign |
0.01 |
R9516:Akap13
|
UTSW |
7 |
75,704,527 (GRCm38) |
missense |
probably benign |
0.01 |
R9523:Akap13
|
UTSW |
7 |
75,643,445 (GRCm38) |
missense |
|
|
R9564:Akap13
|
UTSW |
7 |
75,609,413 (GRCm38) |
missense |
probably benign |
|
R9621:Akap13
|
UTSW |
7 |
75,736,342 (GRCm38) |
missense |
probably benign |
0.09 |
R9686:Akap13
|
UTSW |
7 |
75,586,336 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Akap13
|
UTSW |
7 |
75,730,552 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1177:Akap13
|
UTSW |
7 |
75,615,005 (GRCm38) |
missense |
probably benign |
0.17 |
|