Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
C |
5: 8,984,226 (GRCm39) |
V652A |
probably benign |
Het |
Acvrl1 |
G |
T |
15: 101,038,953 (GRCm39) |
V417L |
probably damaging |
Het |
Add1 |
A |
G |
5: 34,776,715 (GRCm39) |
R479G |
probably benign |
Het |
Adgb |
A |
T |
10: 10,276,318 (GRCm39) |
L350Q |
possibly damaging |
Het |
Adgrl2 |
A |
T |
3: 148,552,506 (GRCm39) |
S666T |
probably benign |
Het |
Amigo3 |
C |
A |
9: 107,931,265 (GRCm39) |
H229Q |
probably benign |
Het |
Ano6 |
G |
C |
15: 95,762,125 (GRCm39) |
Q31H |
possibly damaging |
Het |
Ap4m1 |
G |
A |
5: 138,173,281 (GRCm39) |
D180N |
probably damaging |
Het |
Apc2 |
A |
T |
10: 80,147,574 (GRCm39) |
D876V |
probably damaging |
Het |
Apcdd1 |
T |
A |
18: 63,085,259 (GRCm39) |
Y485* |
probably null |
Het |
Aqp1 |
G |
T |
6: 55,313,836 (GRCm39) |
D121Y |
probably benign |
Het |
Bicd2 |
C |
A |
13: 49,523,085 (GRCm39) |
R141S |
probably benign |
Het |
Brpf3 |
C |
A |
17: 29,025,267 (GRCm39) |
H113Q |
probably benign |
Het |
Cacng2 |
A |
T |
15: 77,897,520 (GRCm39) |
Y96* |
probably null |
Het |
Catsperg1 |
G |
T |
7: 28,910,184 (GRCm39) |
N52K |
possibly damaging |
Het |
Celsr2 |
A |
C |
3: 108,302,311 (GRCm39) |
F2606V |
possibly damaging |
Het |
Cerkl |
A |
T |
2: 79,162,949 (GRCm39) |
N516K |
probably benign |
Het |
Ciita |
G |
A |
16: 10,330,152 (GRCm39) |
R812H |
probably damaging |
Het |
Cldn3 |
T |
A |
5: 135,015,837 (GRCm39) |
L180Q |
probably damaging |
Het |
Cnot6l |
T |
C |
5: 96,225,158 (GRCm39) |
I512V |
probably benign |
Het |
Col5a2 |
A |
T |
1: 45,482,027 (GRCm39) |
D32E |
unknown |
Het |
Coro7 |
A |
G |
16: 4,449,912 (GRCm39) |
V616A |
probably damaging |
Het |
Cyp4f18 |
T |
C |
8: 72,742,498 (GRCm39) |
D494G |
probably benign |
Het |
Ddx39a |
T |
A |
8: 84,449,100 (GRCm39) |
V296E |
probably benign |
Het |
Dgkg |
A |
T |
16: 22,367,440 (GRCm39) |
H593Q |
probably damaging |
Het |
Dhx16 |
T |
C |
17: 36,197,052 (GRCm39) |
L645P |
probably damaging |
Het |
Dnah14 |
A |
G |
1: 181,425,968 (GRCm39) |
M171V |
probably benign |
Het |
Dnhd1 |
G |
A |
7: 105,370,137 (GRCm39) |
V4521I |
probably damaging |
Het |
Dok7 |
A |
T |
5: 35,221,866 (GRCm39) |
M60L |
probably benign |
Het |
Donson |
A |
T |
16: 91,485,599 (GRCm39) |
M1K |
probably null |
Het |
Dsp |
C |
T |
13: 38,376,859 (GRCm39) |
T1548M |
probably benign |
Het |
Dyrk1a |
A |
G |
16: 94,492,902 (GRCm39) |
T712A |
probably damaging |
Het |
Eef2 |
A |
G |
10: 81,017,116 (GRCm39) |
T708A |
probably benign |
Het |
Epn3 |
G |
A |
11: 94,384,606 (GRCm39) |
T289I |
probably benign |
Het |
Fam171a1 |
C |
T |
2: 3,227,509 (GRCm39) |
R881* |
probably null |
Het |
Fat2 |
T |
A |
11: 55,173,130 (GRCm39) |
R2528W |
probably damaging |
Het |
Fbxl9 |
T |
C |
8: 106,039,530 (GRCm39) |
D127G |
probably damaging |
Het |
Fgfr1 |
T |
G |
8: 26,063,855 (GRCm39) |
F707C |
probably damaging |
Het |
Frem2 |
G |
C |
3: 53,562,174 (GRCm39) |
P778A |
probably damaging |
Het |
Ganc |
A |
G |
2: 120,261,080 (GRCm39) |
Y255C |
probably damaging |
Het |
Garin4 |
G |
A |
1: 190,896,550 (GRCm39) |
T31M |
probably benign |
Het |
Ginm1 |
A |
T |
10: 7,653,614 (GRCm39) |
Y65* |
probably null |
Het |
Gm11559 |
T |
A |
11: 99,755,707 (GRCm39) |
C119S |
unknown |
Het |
Gnai1 |
T |
A |
5: 18,494,549 (GRCm39) |
H188L |
|
Het |
H2bc6 |
T |
C |
13: 23,769,906 (GRCm39) |
K12E |
probably benign |
Het |
H6pd |
C |
T |
4: 150,080,807 (GRCm39) |
A13T |
probably benign |
Het |
Hoxd12 |
A |
T |
2: 74,505,590 (GRCm39) |
T54S |
possibly damaging |
Het |
Hs3st5 |
T |
A |
10: 36,709,190 (GRCm39) |
L242M |
probably damaging |
Het |
Il9r |
C |
A |
11: 32,144,389 (GRCm39) |
V139L |
possibly damaging |
Het |
Immt |
A |
G |
6: 71,823,353 (GRCm39) |
D68G |
probably damaging |
Het |
Itsn2 |
A |
G |
12: 4,682,985 (GRCm39) |
I304V |
unknown |
Het |
Lgr4 |
G |
A |
2: 109,826,974 (GRCm39) |
W159* |
probably null |
Het |
Lin52 |
G |
A |
12: 84,504,728 (GRCm39) |
G38S |
probably damaging |
Het |
Lpgat1 |
A |
T |
1: 191,451,565 (GRCm39) |
M64L |
probably benign |
Het |
Lrrc10b |
G |
T |
19: 10,434,142 (GRCm39) |
R180S |
possibly damaging |
Het |
Lrrc36 |
A |
T |
8: 106,176,401 (GRCm39) |
L258F |
possibly damaging |
Het |
Ltbp4 |
T |
A |
7: 27,029,180 (GRCm39) |
Q235L |
unknown |
Het |
Maml2 |
A |
G |
9: 13,532,903 (GRCm39) |
M706V |
|
Het |
Mc5r |
G |
T |
18: 68,472,739 (GRCm39) |
C366F |
probably damaging |
Het |
Mlip |
T |
C |
9: 77,072,124 (GRCm39) |
R244G |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,496,309 (GRCm39) |
R6658S |
probably benign |
Het |
Mup4 |
G |
T |
4: 59,960,046 (GRCm39) |
H73N |
possibly damaging |
Het |
Nf1 |
A |
G |
11: 79,455,769 (GRCm39) |
M565V |
probably benign |
Het |
Nphp1 |
G |
A |
2: 127,603,137 (GRCm39) |
T382I |
possibly damaging |
Het |
Nrcam |
C |
T |
12: 44,610,809 (GRCm39) |
T503I |
possibly damaging |
Het |
Nwd2 |
A |
T |
5: 63,957,752 (GRCm39) |
N361Y |
probably damaging |
Het |
Or10a3 |
A |
T |
7: 108,480,023 (GRCm39) |
H263Q |
probably damaging |
Het |
Or4f15 |
A |
T |
2: 111,813,672 (GRCm39) |
L249* |
probably null |
Het |
Or5ak23 |
A |
T |
2: 85,244,788 (GRCm39) |
V145E |
probably damaging |
Het |
Or6f1 |
A |
G |
7: 85,970,782 (GRCm39) |
I126T |
probably damaging |
Het |
Or7g21 |
A |
G |
9: 19,032,965 (GRCm39) |
Y235C |
probably benign |
Het |
Or8j3 |
A |
G |
2: 86,028,917 (GRCm39) |
Y60H |
probably damaging |
Het |
Or9a7 |
G |
T |
6: 40,521,829 (GRCm39) |
A28E |
probably damaging |
Het |
Orc5 |
A |
G |
5: 22,728,582 (GRCm39) |
F308L |
probably benign |
Het |
Padi1 |
T |
A |
4: 140,559,715 (GRCm39) |
Y54F |
probably benign |
Het |
Parp1 |
A |
G |
1: 180,396,665 (GRCm39) |
K23E |
possibly damaging |
Het |
Pate1 |
A |
T |
9: 35,597,268 (GRCm39) |
V79D |
possibly damaging |
Het |
Pcdh18 |
T |
C |
3: 49,711,309 (GRCm39) |
H2R |
probably benign |
Het |
Pcnx2 |
G |
A |
8: 126,613,822 (GRCm39) |
S543F |
probably damaging |
Het |
Pcp4l1 |
G |
A |
1: 171,002,034 (GRCm39) |
A42V |
possibly damaging |
Het |
Pnkp |
T |
A |
7: 44,509,158 (GRCm39) |
F169L |
probably damaging |
Het |
Ppp6r3 |
A |
T |
19: 3,557,325 (GRCm39) |
N254K |
probably damaging |
Het |
Psd |
A |
G |
19: 46,312,893 (GRCm39) |
L159P |
probably benign |
Het |
Ptprf |
A |
G |
4: 118,088,866 (GRCm39) |
Y646H |
probably damaging |
Het |
Rab3ip |
A |
T |
10: 116,773,538 (GRCm39) |
S92T |
probably benign |
Het |
Rabgef1 |
A |
G |
5: 130,216,192 (GRCm39) |
|
probably benign |
Het |
Ralgapa1 |
C |
A |
12: 55,755,789 (GRCm39) |
W1129L |
probably damaging |
Het |
Rhpn2 |
T |
A |
7: 35,084,888 (GRCm39) |
L594Q |
probably benign |
Het |
Rnf38 |
C |
A |
4: 44,158,989 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,753,080 (GRCm39) |
H1747L |
possibly damaging |
Het |
Sec16a |
A |
G |
2: 26,329,729 (GRCm39) |
L13P |
unknown |
Het |
Spef1l |
A |
T |
7: 139,558,458 (GRCm39) |
|
probably null |
Het |
Sppl3 |
C |
A |
5: 115,220,394 (GRCm39) |
T102K |
probably damaging |
Het |
Srgap2 |
A |
T |
1: 131,219,351 (GRCm39) |
Y264* |
probably null |
Het |
Stxbp2 |
T |
C |
8: 3,691,151 (GRCm39) |
M465T |
|
Het |
Sumf2 |
A |
G |
5: 129,891,551 (GRCm39) |
K305R |
probably benign |
Het |
Susd2 |
T |
A |
10: 75,478,399 (GRCm39) |
Y59F |
probably benign |
Het |
Taco1 |
T |
C |
11: 105,963,443 (GRCm39) |
V198A |
probably benign |
Het |
Tas2r136 |
A |
T |
6: 132,754,869 (GRCm39) |
M86K |
possibly damaging |
Het |
Tbc1d10c |
T |
C |
19: 4,234,897 (GRCm39) |
E388G |
possibly damaging |
Het |
Tmem132c |
C |
T |
5: 127,641,123 (GRCm39) |
T1098I |
possibly damaging |
Het |
Trim3 |
G |
T |
7: 105,267,007 (GRCm39) |
Y457* |
probably null |
Het |
Ttc38 |
A |
G |
15: 85,737,062 (GRCm39) |
T316A |
probably benign |
Het |
Ubqln4 |
T |
A |
3: 88,463,217 (GRCm39) |
N127K |
probably benign |
Het |
Wdr91 |
A |
T |
6: 34,881,561 (GRCm39) |
F262Y |
probably damaging |
Het |
Zdhhc6 |
A |
T |
19: 55,291,187 (GRCm39) |
C343S |
possibly damaging |
Het |
Zfp248 |
A |
G |
6: 118,407,170 (GRCm39) |
C140R |
probably damaging |
Het |
Zfp266 |
T |
C |
9: 20,413,391 (GRCm39) |
T90A |
probably benign |
Het |
Zfp407 |
A |
T |
18: 84,577,167 (GRCm39) |
D1315E |
possibly damaging |
Het |
Zfp644 |
T |
C |
5: 106,786,143 (GRCm39) |
S135G |
probably benign |
Het |
Zscan29 |
A |
T |
2: 120,991,469 (GRCm39) |
I773N |
probably damaging |
Het |
Zswim5 |
T |
A |
4: 116,838,031 (GRCm39) |
V787E |
possibly damaging |
Het |
|
Other mutations in Akap9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00478:Akap9
|
APN |
5 |
4,096,639 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00642:Akap9
|
APN |
5 |
4,010,842 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00786:Akap9
|
APN |
5 |
4,120,522 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00788:Akap9
|
APN |
5 |
4,110,480 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00969:Akap9
|
APN |
5 |
4,051,550 (GRCm39) |
missense |
probably benign |
|
IGL01014:Akap9
|
APN |
5 |
4,018,683 (GRCm39) |
missense |
probably benign |
0.41 |
IGL01302:Akap9
|
APN |
5 |
4,020,711 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01610:Akap9
|
APN |
5 |
4,082,839 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01620:Akap9
|
APN |
5 |
4,010,218 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01862:Akap9
|
APN |
5 |
4,115,856 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01862:Akap9
|
APN |
5 |
4,001,705 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02151:Akap9
|
APN |
5 |
4,082,728 (GRCm39) |
nonsense |
probably null |
|
IGL02635:Akap9
|
APN |
5 |
4,120,500 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02858:Akap9
|
APN |
5 |
4,119,130 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02967:Akap9
|
APN |
5 |
4,026,164 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03064:Akap9
|
APN |
5 |
4,018,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03289:Akap9
|
APN |
5 |
4,127,261 (GRCm39) |
missense |
probably damaging |
1.00 |
Andy
|
UTSW |
5 |
4,011,764 (GRCm39) |
nonsense |
probably null |
|
blimey
|
UTSW |
5 |
4,120,397 (GRCm39) |
nonsense |
probably null |
|
hoarder
|
UTSW |
5 |
4,119,089 (GRCm39) |
missense |
probably benign |
0.00 |
marinarum
|
UTSW |
5 |
4,063,875 (GRCm39) |
nonsense |
probably null |
|
miser
|
UTSW |
5 |
4,096,064 (GRCm39) |
missense |
probably benign |
0.13 |
naviculus
|
UTSW |
5 |
4,010,865 (GRCm39) |
missense |
probably damaging |
0.98 |
thrifty
|
UTSW |
5 |
4,026,209 (GRCm39) |
missense |
probably damaging |
0.99 |
wee_one
|
UTSW |
5 |
4,093,925 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Akap9
|
UTSW |
5 |
4,031,214 (GRCm39) |
unclassified |
probably benign |
|
PIT1430001:Akap9
|
UTSW |
5 |
4,079,849 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4366001:Akap9
|
UTSW |
5 |
4,096,221 (GRCm39) |
missense |
probably benign |
0.24 |
R0088:Akap9
|
UTSW |
5 |
4,011,946 (GRCm39) |
missense |
probably benign |
0.22 |
R0309:Akap9
|
UTSW |
5 |
4,119,038 (GRCm39) |
missense |
probably benign |
0.01 |
R0387:Akap9
|
UTSW |
5 |
4,001,678 (GRCm39) |
splice site |
probably benign |
|
R0440:Akap9
|
UTSW |
5 |
4,114,569 (GRCm39) |
missense |
probably damaging |
0.99 |
R0441:Akap9
|
UTSW |
5 |
4,011,714 (GRCm39) |
missense |
probably benign |
0.15 |
R0491:Akap9
|
UTSW |
5 |
4,022,851 (GRCm39) |
unclassified |
probably benign |
|
R0501:Akap9
|
UTSW |
5 |
4,020,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R0507:Akap9
|
UTSW |
5 |
4,119,043 (GRCm39) |
missense |
probably benign |
0.41 |
R0544:Akap9
|
UTSW |
5 |
4,119,185 (GRCm39) |
missense |
probably benign |
0.22 |
R0581:Akap9
|
UTSW |
5 |
4,100,620 (GRCm39) |
missense |
probably benign |
0.03 |
R0611:Akap9
|
UTSW |
5 |
4,004,870 (GRCm39) |
missense |
probably benign |
0.00 |
R0620:Akap9
|
UTSW |
5 |
4,114,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R0639:Akap9
|
UTSW |
5 |
4,110,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R0932:Akap9
|
UTSW |
5 |
4,096,492 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0944:Akap9
|
UTSW |
5 |
4,114,742 (GRCm39) |
splice site |
probably null |
|
R1101:Akap9
|
UTSW |
5 |
4,096,205 (GRCm39) |
missense |
probably benign |
0.00 |
R1159:Akap9
|
UTSW |
5 |
4,010,865 (GRCm39) |
missense |
probably damaging |
0.98 |
R1170:Akap9
|
UTSW |
5 |
4,105,671 (GRCm39) |
missense |
probably benign |
|
R1185:Akap9
|
UTSW |
5 |
3,998,783 (GRCm39) |
missense |
probably benign |
0.13 |
R1185:Akap9
|
UTSW |
5 |
3,998,783 (GRCm39) |
missense |
probably benign |
0.13 |
R1185:Akap9
|
UTSW |
5 |
3,998,783 (GRCm39) |
missense |
probably benign |
0.13 |
R1453:Akap9
|
UTSW |
5 |
4,025,614 (GRCm39) |
splice site |
probably null |
|
R1551:Akap9
|
UTSW |
5 |
4,119,174 (GRCm39) |
missense |
probably benign |
0.02 |
R1608:Akap9
|
UTSW |
5 |
4,011,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R1652:Akap9
|
UTSW |
5 |
4,127,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1659:Akap9
|
UTSW |
5 |
4,114,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Akap9
|
UTSW |
5 |
4,089,345 (GRCm39) |
critical splice donor site |
probably null |
|
R1719:Akap9
|
UTSW |
5 |
4,007,645 (GRCm39) |
nonsense |
probably null |
|
R1720:Akap9
|
UTSW |
5 |
4,022,791 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1757:Akap9
|
UTSW |
5 |
4,051,667 (GRCm39) |
missense |
probably benign |
0.41 |
R1872:Akap9
|
UTSW |
5 |
4,051,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R1876:Akap9
|
UTSW |
5 |
4,011,809 (GRCm39) |
missense |
probably benign |
0.28 |
R1881:Akap9
|
UTSW |
5 |
4,100,173 (GRCm39) |
missense |
probably benign |
|
R1950:Akap9
|
UTSW |
5 |
4,010,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Akap9
|
UTSW |
5 |
4,022,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R1993:Akap9
|
UTSW |
5 |
4,088,520 (GRCm39) |
splice site |
probably null |
|
R2008:Akap9
|
UTSW |
5 |
4,010,131 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2020:Akap9
|
UTSW |
5 |
4,011,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Akap9
|
UTSW |
5 |
4,025,685 (GRCm39) |
nonsense |
probably null |
|
R2061:Akap9
|
UTSW |
5 |
4,011,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Akap9
|
UTSW |
5 |
4,094,847 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2135:Akap9
|
UTSW |
5 |
4,114,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R2225:Akap9
|
UTSW |
5 |
4,127,271 (GRCm39) |
missense |
probably damaging |
0.96 |
R2232:Akap9
|
UTSW |
5 |
4,096,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R2424:Akap9
|
UTSW |
5 |
4,115,279 (GRCm39) |
missense |
probably damaging |
0.97 |
R2483:Akap9
|
UTSW |
5 |
4,026,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2879:Akap9
|
UTSW |
5 |
4,026,353 (GRCm39) |
intron |
probably benign |
|
R3622:Akap9
|
UTSW |
5 |
4,026,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3623:Akap9
|
UTSW |
5 |
4,026,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3624:Akap9
|
UTSW |
5 |
4,026,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3722:Akap9
|
UTSW |
5 |
4,120,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Akap9
|
UTSW |
5 |
4,004,410 (GRCm39) |
missense |
probably benign |
0.00 |
R3919:Akap9
|
UTSW |
5 |
4,011,764 (GRCm39) |
nonsense |
probably null |
|
R4023:Akap9
|
UTSW |
5 |
4,042,077 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4093:Akap9
|
UTSW |
5 |
4,093,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R4434:Akap9
|
UTSW |
5 |
4,082,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R4529:Akap9
|
UTSW |
5 |
4,093,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4530:Akap9
|
UTSW |
5 |
4,093,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4532:Akap9
|
UTSW |
5 |
4,093,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4533:Akap9
|
UTSW |
5 |
4,093,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4585:Akap9
|
UTSW |
5 |
4,026,151 (GRCm39) |
missense |
probably benign |
0.00 |
R4586:Akap9
|
UTSW |
5 |
4,026,151 (GRCm39) |
missense |
probably benign |
0.00 |
R4655:Akap9
|
UTSW |
5 |
4,096,403 (GRCm39) |
missense |
probably benign |
0.14 |
R4676:Akap9
|
UTSW |
5 |
4,114,515 (GRCm39) |
nonsense |
probably null |
|
R4676:Akap9
|
UTSW |
5 |
4,082,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Akap9
|
UTSW |
5 |
4,105,339 (GRCm39) |
missense |
probably benign |
|
R4731:Akap9
|
UTSW |
5 |
4,012,266 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4732:Akap9
|
UTSW |
5 |
4,063,901 (GRCm39) |
missense |
probably damaging |
0.98 |
R4733:Akap9
|
UTSW |
5 |
4,063,901 (GRCm39) |
missense |
probably damaging |
0.98 |
R4743:Akap9
|
UTSW |
5 |
4,011,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Akap9
|
UTSW |
5 |
4,018,737 (GRCm39) |
missense |
probably benign |
0.41 |
R4756:Akap9
|
UTSW |
5 |
4,051,418 (GRCm39) |
missense |
probably damaging |
0.99 |
R4757:Akap9
|
UTSW |
5 |
4,058,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Akap9
|
UTSW |
5 |
4,084,916 (GRCm39) |
intron |
probably benign |
|
R4937:Akap9
|
UTSW |
5 |
4,100,145 (GRCm39) |
splice site |
probably null |
|
R4960:Akap9
|
UTSW |
5 |
4,007,664 (GRCm39) |
missense |
probably benign |
0.15 |
R4974:Akap9
|
UTSW |
5 |
4,011,466 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5101:Akap9
|
UTSW |
5 |
4,051,748 (GRCm39) |
missense |
probably damaging |
0.96 |
R5160:Akap9
|
UTSW |
5 |
4,080,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5200:Akap9
|
UTSW |
5 |
4,010,734 (GRCm39) |
missense |
probably benign |
0.00 |
R5245:Akap9
|
UTSW |
5 |
4,026,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R5293:Akap9
|
UTSW |
5 |
3,998,687 (GRCm39) |
missense |
probably damaging |
0.99 |
R5408:Akap9
|
UTSW |
5 |
4,108,458 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5507:Akap9
|
UTSW |
5 |
4,018,683 (GRCm39) |
missense |
probably benign |
0.41 |
R5517:Akap9
|
UTSW |
5 |
4,051,665 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5579:Akap9
|
UTSW |
5 |
4,114,714 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5619:Akap9
|
UTSW |
5 |
4,004,760 (GRCm39) |
intron |
probably benign |
|
R5645:Akap9
|
UTSW |
5 |
4,100,590 (GRCm39) |
missense |
probably benign |
0.09 |
R5669:Akap9
|
UTSW |
5 |
4,100,540 (GRCm39) |
nonsense |
probably null |
|
R5686:Akap9
|
UTSW |
5 |
4,021,926 (GRCm39) |
missense |
probably benign |
0.00 |
R5697:Akap9
|
UTSW |
5 |
4,010,170 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5821:Akap9
|
UTSW |
5 |
4,096,064 (GRCm39) |
missense |
probably benign |
0.13 |
R5875:Akap9
|
UTSW |
5 |
4,127,285 (GRCm39) |
missense |
probably benign |
0.01 |
R5897:Akap9
|
UTSW |
5 |
4,127,904 (GRCm39) |
missense |
probably benign |
0.23 |
R5999:Akap9
|
UTSW |
5 |
4,093,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R6025:Akap9
|
UTSW |
5 |
4,082,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R6078:Akap9
|
UTSW |
5 |
4,117,924 (GRCm39) |
critical splice donor site |
probably null |
|
R6138:Akap9
|
UTSW |
5 |
4,117,924 (GRCm39) |
critical splice donor site |
probably null |
|
R6225:Akap9
|
UTSW |
5 |
4,012,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R6243:Akap9
|
UTSW |
5 |
4,115,000 (GRCm39) |
splice site |
probably null |
|
R6326:Akap9
|
UTSW |
5 |
4,012,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R6564:Akap9
|
UTSW |
5 |
4,078,491 (GRCm39) |
missense |
probably damaging |
0.98 |
R6617:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R6625:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R6632:Akap9
|
UTSW |
5 |
4,063,842 (GRCm39) |
splice site |
probably null |
|
R6677:Akap9
|
UTSW |
5 |
4,079,869 (GRCm39) |
missense |
probably benign |
0.21 |
R6717:Akap9
|
UTSW |
5 |
4,114,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R6893:Akap9
|
UTSW |
5 |
4,011,709 (GRCm39) |
missense |
probably benign |
0.32 |
R6915:Akap9
|
UTSW |
5 |
4,010,551 (GRCm39) |
missense |
probably benign |
0.03 |
R6938:Akap9
|
UTSW |
5 |
4,096,628 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6972:Akap9
|
UTSW |
5 |
4,096,699 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6973:Akap9
|
UTSW |
5 |
4,096,699 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6993:Akap9
|
UTSW |
5 |
4,115,866 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7032:Akap9
|
UTSW |
5 |
4,004,896 (GRCm39) |
missense |
probably benign |
|
R7164:Akap9
|
UTSW |
5 |
4,110,364 (GRCm39) |
missense |
probably damaging |
0.96 |
R7170:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7192:Akap9
|
UTSW |
5 |
4,055,723 (GRCm39) |
splice site |
probably null |
|
R7284:Akap9
|
UTSW |
5 |
4,006,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Akap9
|
UTSW |
5 |
4,082,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Akap9
|
UTSW |
5 |
4,054,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Akap9
|
UTSW |
5 |
4,096,364 (GRCm39) |
missense |
probably damaging |
0.99 |
R7455:Akap9
|
UTSW |
5 |
4,022,792 (GRCm39) |
missense |
probably benign |
0.03 |
R7482:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7489:Akap9
|
UTSW |
5 |
4,054,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7525:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7528:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7576:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7577:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7578:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7610:Akap9
|
UTSW |
5 |
4,007,677 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7658:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7754:Akap9
|
UTSW |
5 |
4,096,736 (GRCm39) |
missense |
probably benign |
0.03 |
R7818:Akap9
|
UTSW |
5 |
4,063,875 (GRCm39) |
nonsense |
probably null |
|
R7979:Akap9
|
UTSW |
5 |
4,100,381 (GRCm39) |
missense |
probably benign |
|
R7991:Akap9
|
UTSW |
5 |
4,114,949 (GRCm39) |
splice site |
probably null |
|
R8036:Akap9
|
UTSW |
5 |
4,120,397 (GRCm39) |
nonsense |
probably null |
|
R8054:Akap9
|
UTSW |
5 |
4,088,707 (GRCm39) |
critical splice donor site |
probably null |
|
R8116:Akap9
|
UTSW |
5 |
4,111,183 (GRCm39) |
missense |
probably benign |
0.04 |
R8150:Akap9
|
UTSW |
5 |
4,011,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R8234:Akap9
|
UTSW |
5 |
4,094,845 (GRCm39) |
missense |
probably benign |
0.18 |
R8348:Akap9
|
UTSW |
5 |
3,998,897 (GRCm39) |
critical splice donor site |
probably null |
|
R8365:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R8366:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R8448:Akap9
|
UTSW |
5 |
3,998,897 (GRCm39) |
critical splice donor site |
probably null |
|
R8466:Akap9
|
UTSW |
5 |
4,088,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R8772:Akap9
|
UTSW |
5 |
4,096,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8881:Akap9
|
UTSW |
5 |
4,011,279 (GRCm39) |
missense |
|
|
R8937:Akap9
|
UTSW |
5 |
4,094,048 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8956:Akap9
|
UTSW |
5 |
3,998,805 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9000:Akap9
|
UTSW |
5 |
4,105,650 (GRCm39) |
missense |
probably benign |
|
R9049:Akap9
|
UTSW |
5 |
4,114,597 (GRCm39) |
missense |
|
|
R9074:Akap9
|
UTSW |
5 |
4,127,959 (GRCm39) |
missense |
probably benign |
0.40 |
R9124:Akap9
|
UTSW |
5 |
4,111,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R9129:Akap9
|
UTSW |
5 |
4,119,089 (GRCm39) |
missense |
probably benign |
0.00 |
R9371:Akap9
|
UTSW |
5 |
4,011,852 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9424:Akap9
|
UTSW |
5 |
4,012,224 (GRCm39) |
nonsense |
probably null |
|
R9424:Akap9
|
UTSW |
5 |
4,012,223 (GRCm39) |
nonsense |
probably null |
|
R9509:Akap9
|
UTSW |
5 |
4,096,349 (GRCm39) |
missense |
probably benign |
|
R9515:Akap9
|
UTSW |
5 |
4,105,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R9567:Akap9
|
UTSW |
5 |
4,127,311 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9587:Akap9
|
UTSW |
5 |
4,119,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R9619:Akap9
|
UTSW |
5 |
4,094,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9635:Akap9
|
UTSW |
5 |
4,100,545 (GRCm39) |
missense |
probably benign |
0.20 |
R9680:Akap9
|
UTSW |
5 |
4,011,587 (GRCm39) |
missense |
probably benign |
0.03 |
R9691:Akap9
|
UTSW |
5 |
4,010,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R9726:Akap9
|
UTSW |
5 |
4,053,757 (GRCm39) |
missense |
probably benign |
0.39 |
U15987:Akap9
|
UTSW |
5 |
4,117,924 (GRCm39) |
critical splice donor site |
probably null |
|
X0026:Akap9
|
UTSW |
5 |
4,064,039 (GRCm39) |
missense |
probably damaging |
1.00 |
X0057:Akap9
|
UTSW |
5 |
4,025,598 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Akap9
|
UTSW |
5 |
4,012,251 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Akap9
|
UTSW |
5 |
4,096,189 (GRCm39) |
missense |
probably damaging |
1.00 |
|