Other mutations in this stock |
Total: 135 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
C |
T |
12: 71,236,420 (GRCm39) |
A1257V |
possibly damaging |
Het |
Aldh8a1 |
T |
C |
10: 21,271,662 (GRCm39) |
S463P |
probably damaging |
Het |
Angptl1 |
T |
G |
1: 156,672,388 (GRCm39) |
D71E |
probably benign |
Het |
Ano1 |
A |
G |
7: 144,165,112 (GRCm39) |
S649P |
possibly damaging |
Het |
Arhgef40 |
A |
G |
14: 52,227,556 (GRCm39) |
E434G |
probably damaging |
Het |
Asb15 |
A |
T |
6: 24,566,292 (GRCm39) |
D415V |
probably damaging |
Het |
Baz2b |
T |
A |
2: 59,744,387 (GRCm39) |
T1373S |
possibly damaging |
Het |
Bcas1 |
T |
C |
2: 170,220,806 (GRCm39) |
D324G |
probably damaging |
Het |
Bfsp1 |
C |
T |
2: 143,669,391 (GRCm39) |
R396Q |
probably benign |
Het |
Bmi1 |
G |
A |
2: 18,687,143 (GRCm39) |
|
probably benign |
Het |
Bpifb9b |
T |
A |
2: 154,156,026 (GRCm39) |
|
probably null |
Het |
Brd9 |
A |
G |
13: 74,086,574 (GRCm39) |
E25G |
probably damaging |
Het |
Btbd7 |
A |
T |
12: 102,804,046 (GRCm39) |
C331* |
probably null |
Het |
Ccdc198 |
A |
T |
14: 49,470,351 (GRCm39) |
N189K |
probably benign |
Het |
Cdh26 |
T |
C |
2: 178,091,614 (GRCm39) |
S58P |
probably benign |
Het |
Cenpj |
T |
C |
14: 56,791,175 (GRCm39) |
D328G |
probably damaging |
Het |
Cherp |
T |
C |
8: 73,222,241 (GRCm39) |
D255G |
probably damaging |
Het |
Clec5a |
T |
A |
6: 40,562,165 (GRCm39) |
|
probably benign |
Het |
Cntnap2 |
T |
C |
6: 46,506,969 (GRCm39) |
|
probably benign |
Het |
Col7a1 |
G |
A |
9: 108,795,532 (GRCm39) |
G1529E |
unknown |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Cyp2a22 |
C |
A |
7: 26,637,195 (GRCm39) |
E196D |
probably benign |
Het |
Cyp4f18 |
T |
A |
8: 72,762,898 (GRCm39) |
H63L |
probably damaging |
Het |
Dclk2 |
A |
T |
3: 86,732,049 (GRCm39) |
|
probably null |
Het |
Ddx6 |
T |
A |
9: 44,524,170 (GRCm39) |
D82E |
probably damaging |
Het |
Defb42 |
A |
G |
14: 63,285,790 (GRCm39) |
I57V |
probably benign |
Het |
Dennd5a |
A |
G |
7: 109,500,296 (GRCm39) |
F943S |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,671,905 (GRCm39) |
|
probably null |
Het |
Disp2 |
A |
T |
2: 118,620,935 (GRCm39) |
S556C |
probably damaging |
Het |
Dnah12 |
A |
T |
14: 26,455,725 (GRCm39) |
D816V |
probably damaging |
Het |
Dpy19l3 |
T |
C |
7: 35,452,167 (GRCm39) |
|
probably benign |
Het |
Efcab11 |
T |
C |
12: 99,685,321 (GRCm39) |
D151G |
probably damaging |
Het |
Ehbp1 |
T |
C |
11: 22,096,592 (GRCm39) |
D299G |
probably benign |
Het |
Evl |
G |
T |
12: 108,652,365 (GRCm39) |
R359L |
probably damaging |
Het |
Fasn |
T |
G |
11: 120,707,472 (GRCm39) |
N799T |
probably benign |
Het |
Fbxo3 |
T |
G |
2: 103,885,311 (GRCm39) |
N388K |
probably damaging |
Het |
Fbxw14 |
A |
T |
9: 109,103,592 (GRCm39) |
F40Y |
possibly damaging |
Het |
Fbxw22 |
A |
G |
9: 109,213,009 (GRCm39) |
F313L |
probably damaging |
Het |
Fer1l4 |
T |
C |
2: 155,873,220 (GRCm39) |
K1287E |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,634,968 (GRCm39) |
|
probably null |
Het |
Fry |
A |
T |
5: 150,402,328 (GRCm39) |
T790S |
probably benign |
Het |
Fut8 |
G |
T |
12: 77,521,818 (GRCm39) |
A486S |
probably damaging |
Het |
Gfra1 |
A |
T |
19: 58,255,522 (GRCm39) |
S308R |
probably damaging |
Het |
Gm13030 |
T |
A |
4: 138,601,239 (GRCm39) |
|
probably benign |
Het |
Gm37150 |
C |
T |
9: 72,292,772 (GRCm39) |
|
noncoding transcript |
Het |
Gm6788 |
C |
T |
19: 28,740,664 (GRCm39) |
|
noncoding transcript |
Het |
Gm8122 |
T |
C |
14: 43,091,573 (GRCm39) |
N65S |
unknown |
Het |
Gnb4 |
C |
T |
3: 32,639,236 (GRCm39) |
|
probably benign |
Het |
Gprin1 |
G |
T |
13: 54,885,886 (GRCm39) |
P796Q |
probably damaging |
Het |
Grin1 |
A |
G |
2: 25,188,565 (GRCm39) |
|
probably benign |
Het |
Helz2 |
T |
C |
2: 180,874,231 (GRCm39) |
R2088G |
possibly damaging |
Het |
Hsd3b9 |
C |
T |
3: 98,357,845 (GRCm39) |
V56M |
probably damaging |
Het |
Ighv6-6 |
C |
A |
12: 114,398,595 (GRCm39) |
R57L |
probably damaging |
Het |
Inhca |
A |
C |
9: 103,129,054 (GRCm39) |
Y235* |
probably null |
Het |
Inpp5f |
A |
T |
7: 128,286,840 (GRCm39) |
D573V |
probably damaging |
Het |
Iqgap3 |
T |
A |
3: 88,008,834 (GRCm39) |
I643K |
possibly damaging |
Het |
Itga11 |
C |
A |
9: 62,659,530 (GRCm39) |
Y427* |
probably null |
Het |
Kbtbd8 |
T |
G |
6: 95,103,515 (GRCm39) |
M388R |
possibly damaging |
Het |
Kif1a |
T |
A |
1: 93,002,700 (GRCm39) |
E233V |
probably benign |
Het |
Krt10 |
T |
C |
11: 99,278,334 (GRCm39) |
N275S |
probably damaging |
Het |
Lrrc3 |
T |
C |
10: 77,737,253 (GRCm39) |
D61G |
probably benign |
Het |
Mapk8ip3 |
A |
G |
17: 25,128,127 (GRCm39) |
S377P |
possibly damaging |
Het |
Mccc1 |
A |
G |
3: 36,051,703 (GRCm39) |
L32S |
probably benign |
Het |
Meis1 |
T |
C |
11: 18,959,222 (GRCm39) |
|
probably benign |
Het |
Mmp11 |
C |
T |
10: 75,761,419 (GRCm39) |
A31T |
probably damaging |
Het |
Mthfsl |
A |
C |
9: 88,597,550 (GRCm39) |
L67V |
probably damaging |
Het |
Myo1c |
T |
G |
11: 75,547,135 (GRCm39) |
M1R |
probably null |
Het |
N4bp2 |
T |
A |
5: 65,960,847 (GRCm39) |
M506K |
probably damaging |
Het |
Nfix |
T |
C |
8: 85,498,458 (GRCm39) |
I172V |
probably benign |
Het |
Nid1 |
A |
G |
13: 13,674,171 (GRCm39) |
E850G |
possibly damaging |
Het |
Nlrp9c |
T |
C |
7: 26,083,885 (GRCm39) |
T565A |
probably benign |
Het |
Nomo1 |
T |
C |
7: 45,693,656 (GRCm39) |
F163L |
probably benign |
Het |
Nsd1 |
T |
C |
13: 55,395,681 (GRCm39) |
V1197A |
possibly damaging |
Het |
Nsd1 |
A |
G |
13: 55,424,341 (GRCm39) |
T1463A |
probably benign |
Het |
Nsf |
G |
A |
11: 103,801,185 (GRCm39) |
|
probably benign |
Het |
Or3a1b |
A |
T |
11: 74,012,705 (GRCm39) |
I197F |
probably benign |
Het |
Or4k51 |
A |
T |
2: 111,584,725 (GRCm39) |
I44F |
probably benign |
Het |
Or5an1c |
A |
G |
19: 12,218,737 (GRCm39) |
V96A |
probably benign |
Het |
Or5b106 |
T |
A |
19: 13,123,355 (GRCm39) |
I223L |
possibly damaging |
Het |
Or8k33 |
A |
G |
2: 86,384,399 (GRCm39) |
L23P |
probably damaging |
Het |
Or9g10 |
T |
C |
2: 85,584,465 (GRCm39) |
|
probably benign |
Het |
Pcdha6 |
T |
A |
18: 37,101,510 (GRCm39) |
D234E |
probably damaging |
Het |
Pcnx1 |
C |
A |
12: 82,021,269 (GRCm39) |
F1425L |
probably benign |
Het |
Pdzd9 |
T |
G |
7: 120,269,391 (GRCm39) |
N10T |
possibly damaging |
Het |
Pex6 |
A |
T |
17: 47,024,982 (GRCm39) |
H345L |
probably damaging |
Het |
Pfkfb3 |
G |
A |
2: 11,495,109 (GRCm39) |
Q100* |
probably null |
Het |
Pgm2 |
G |
A |
5: 64,258,291 (GRCm39) |
G92E |
probably damaging |
Het |
Pip4k2c |
T |
C |
10: 127,035,196 (GRCm39) |
T391A |
possibly damaging |
Het |
Plcxd2 |
C |
T |
16: 45,800,941 (GRCm39) |
W94* |
probably null |
Het |
Ppm1k |
T |
A |
6: 57,487,762 (GRCm39) |
N354Y |
probably damaging |
Het |
Prkcg |
T |
G |
7: 3,378,781 (GRCm39) |
Y624* |
probably null |
Het |
Rabep2 |
T |
C |
7: 126,044,094 (GRCm39) |
S517P |
probably damaging |
Het |
Rabgap1l |
A |
G |
1: 160,269,412 (GRCm39) |
I717T |
probably benign |
Het |
Rasef |
A |
G |
4: 73,649,696 (GRCm39) |
C484R |
probably damaging |
Het |
Rdh19 |
A |
G |
10: 127,686,113 (GRCm39) |
D75G |
probably benign |
Het |
Rpl21-ps10 |
T |
C |
3: 38,161,617 (GRCm39) |
|
noncoding transcript |
Het |
Rsl1d1 |
A |
T |
16: 11,017,593 (GRCm39) |
|
probably null |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Rwdd1 |
T |
C |
10: 33,885,074 (GRCm39) |
D62G |
possibly damaging |
Het |
Scin |
T |
A |
12: 40,119,373 (GRCm39) |
I552F |
possibly damaging |
Het |
Scn3a |
T |
C |
2: 65,291,799 (GRCm39) |
N1649S |
probably damaging |
Het |
Slc20a2 |
C |
T |
8: 23,051,020 (GRCm39) |
S351L |
probably damaging |
Het |
Slc24a1 |
A |
T |
9: 64,855,213 (GRCm39) |
F565I |
unknown |
Het |
Slc4a1 |
A |
G |
11: 102,243,279 (GRCm39) |
V784A |
probably damaging |
Het |
Slf2 |
T |
G |
19: 44,960,100 (GRCm39) |
D1022E |
probably damaging |
Het |
Sox6 |
T |
C |
7: 115,076,199 (GRCm39) |
D814G |
probably damaging |
Het |
Spata4 |
T |
C |
8: 55,055,471 (GRCm39) |
|
probably null |
Het |
Spats2l |
A |
T |
1: 57,941,347 (GRCm39) |
K202M |
probably damaging |
Het |
Speer4b |
C |
T |
5: 27,705,134 (GRCm39) |
E80K |
probably benign |
Het |
Sqle |
T |
G |
15: 59,193,218 (GRCm39) |
Y198* |
probably null |
Het |
Srek1 |
T |
C |
13: 103,889,194 (GRCm39) |
|
probably benign |
Het |
Srek1 |
T |
C |
13: 103,889,071 (GRCm39) |
|
probably benign |
Het |
St14 |
G |
A |
9: 31,019,960 (GRCm39) |
R50* |
probably null |
Het |
Tcaf1 |
A |
G |
6: 42,652,130 (GRCm39) |
V784A |
probably damaging |
Het |
Tfr2 |
C |
T |
5: 137,581,673 (GRCm39) |
R587W |
probably damaging |
Het |
Tmpo |
A |
G |
10: 90,985,411 (GRCm39) |
V357A |
probably damaging |
Het |
Trrap |
A |
T |
5: 144,742,545 (GRCm39) |
I1101F |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ttpal |
G |
A |
2: 163,449,397 (GRCm39) |
R84H |
probably damaging |
Het |
Tyk2 |
T |
C |
9: 21,022,433 (GRCm39) |
T799A |
probably benign |
Het |
Ugt1a10 |
A |
T |
1: 87,983,646 (GRCm39) |
D148V |
probably damaging |
Het |
Usp29 |
C |
T |
7: 6,964,504 (GRCm39) |
P116S |
probably benign |
Het |
Usp8 |
A |
T |
2: 126,562,060 (GRCm39) |
K85* |
probably null |
Het |
Usp9y |
C |
T |
Y: 1,316,735 (GRCm39) |
R1938H |
probably damaging |
Het |
Vmn1r90 |
T |
G |
7: 14,295,950 (GRCm39) |
R49S |
possibly damaging |
Het |
Vmn2r71 |
C |
A |
7: 85,270,476 (GRCm39) |
N547K |
probably damaging |
Het |
Vps45 |
T |
C |
3: 95,926,943 (GRCm39) |
T535A |
probably damaging |
Het |
Yars1 |
A |
T |
4: 129,104,384 (GRCm39) |
|
probably benign |
Het |
Zfp114 |
T |
C |
7: 23,877,290 (GRCm39) |
L44P |
probably damaging |
Het |
Zfp36l2 |
A |
G |
17: 84,493,690 (GRCm39) |
|
probably benign |
Het |
Zfp512 |
T |
C |
5: 31,634,209 (GRCm39) |
S407P |
probably damaging |
Het |
Zfp574 |
C |
T |
7: 24,780,151 (GRCm39) |
P391L |
probably damaging |
Het |
Zfp607a |
T |
G |
7: 27,577,985 (GRCm39) |
C352G |
probably benign |
Het |
Zfp791 |
T |
A |
8: 85,837,580 (GRCm39) |
I95L |
probably benign |
Het |
Zfr |
A |
C |
15: 12,162,198 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ank2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01298:Ank2
|
APN |
3 |
126,753,369 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01652:Ank2
|
APN |
3 |
126,726,690 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01969:Ank2
|
APN |
3 |
126,746,872 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02122:Ank2
|
APN |
3 |
126,731,523 (GRCm39) |
splice site |
probably benign |
|
IGL02537:Ank2
|
APN |
3 |
126,749,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02858:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02981:Ank2
|
APN |
3 |
126,728,211 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02981:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03024:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03074:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03111:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03129:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03174:Ank2
|
APN |
3 |
126,733,744 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03177:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03185:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03188:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03242:Ank2
|
APN |
3 |
126,722,454 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03244:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03248:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03285:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03304:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03358:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03380:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03389:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03400:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03409:Ank2
|
APN |
3 |
126,749,519 (GRCm39) |
missense |
probably damaging |
1.00 |
ballast
|
UTSW |
3 |
126,736,782 (GRCm39) |
missense |
unknown |
|
Chain
|
UTSW |
3 |
126,740,587 (GRCm39) |
intron |
probably benign |
|
Deadman
|
UTSW |
3 |
126,723,471 (GRCm39) |
missense |
probably benign |
0.19 |
drag
|
UTSW |
3 |
126,797,631 (GRCm39) |
missense |
probably damaging |
1.00 |
mooring
|
UTSW |
3 |
126,728,226 (GRCm39) |
missense |
possibly damaging |
0.73 |
Treasure
|
UTSW |
3 |
126,740,398 (GRCm39) |
missense |
unknown |
|
Windlass
|
UTSW |
3 |
126,739,798 (GRCm39) |
missense |
probably benign |
|
R0033:Ank2
|
UTSW |
3 |
126,898,397 (GRCm39) |
splice site |
probably benign |
|
R0042:Ank2
|
UTSW |
3 |
126,730,280 (GRCm39) |
missense |
probably damaging |
0.99 |
R0042:Ank2
|
UTSW |
3 |
126,730,280 (GRCm39) |
missense |
probably damaging |
0.99 |
R0079:Ank2
|
UTSW |
3 |
126,728,264 (GRCm39) |
missense |
probably benign |
0.01 |
R0423:Ank2
|
UTSW |
3 |
126,723,509 (GRCm39) |
nonsense |
probably null |
|
R0699:Ank2
|
UTSW |
3 |
126,723,478 (GRCm39) |
missense |
probably benign |
0.00 |
R0724:Ank2
|
UTSW |
3 |
126,755,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R0990:Ank2
|
UTSW |
3 |
126,728,315 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1450:Ank2
|
UTSW |
3 |
126,750,951 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1500:Ank2
|
UTSW |
3 |
126,726,631 (GRCm39) |
missense |
probably benign |
|
R1702:Ank2
|
UTSW |
3 |
126,749,548 (GRCm39) |
missense |
probably benign |
0.00 |
R1703:Ank2
|
UTSW |
3 |
126,723,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1710:Ank2
|
UTSW |
3 |
126,726,709 (GRCm39) |
nonsense |
probably null |
|
R1743:Ank2
|
UTSW |
3 |
126,722,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R1775:Ank2
|
UTSW |
3 |
126,728,196 (GRCm39) |
missense |
probably benign |
0.00 |
R1852:Ank2
|
UTSW |
3 |
126,791,500 (GRCm39) |
critical splice donor site |
probably null |
|
R2198:Ank2
|
UTSW |
3 |
126,728,226 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2892:Ank2
|
UTSW |
3 |
127,041,892 (GRCm39) |
splice site |
probably null |
|
R2893:Ank2
|
UTSW |
3 |
127,041,892 (GRCm39) |
splice site |
probably null |
|
R2894:Ank2
|
UTSW |
3 |
127,041,892 (GRCm39) |
splice site |
probably null |
|
R3148:Ank2
|
UTSW |
3 |
126,726,724 (GRCm39) |
missense |
probably benign |
0.00 |
R3776:Ank2
|
UTSW |
3 |
126,735,911 (GRCm39) |
intron |
probably benign |
|
R3784:Ank2
|
UTSW |
3 |
126,746,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R3856:Ank2
|
UTSW |
3 |
126,723,493 (GRCm39) |
missense |
probably benign |
0.00 |
R3906:Ank2
|
UTSW |
3 |
126,810,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Ank2
|
UTSW |
3 |
126,810,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R3953:Ank2
|
UTSW |
3 |
126,781,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R3963:Ank2
|
UTSW |
3 |
126,728,245 (GRCm39) |
missense |
probably benign |
|
R4367:Ank2
|
UTSW |
3 |
126,739,798 (GRCm39) |
missense |
probably benign |
|
R4414:Ank2
|
UTSW |
3 |
127,019,411 (GRCm39) |
critical splice donor site |
probably null |
|
R4432:Ank2
|
UTSW |
3 |
126,741,455 (GRCm39) |
intron |
probably benign |
|
R4433:Ank2
|
UTSW |
3 |
126,741,455 (GRCm39) |
intron |
probably benign |
|
R4579:Ank2
|
UTSW |
3 |
126,752,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4597:Ank2
|
UTSW |
3 |
126,781,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4603:Ank2
|
UTSW |
3 |
126,825,665 (GRCm39) |
missense |
probably benign |
0.00 |
R4729:Ank2
|
UTSW |
3 |
126,770,545 (GRCm39) |
nonsense |
probably null |
|
R4815:Ank2
|
UTSW |
3 |
126,730,410 (GRCm39) |
missense |
probably benign |
|
R4826:Ank2
|
UTSW |
3 |
126,749,650 (GRCm39) |
missense |
probably benign |
0.35 |
R4871:Ank2
|
UTSW |
3 |
126,753,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R4880:Ank2
|
UTSW |
3 |
126,840,475 (GRCm39) |
splice site |
probably null |
|
R4935:Ank2
|
UTSW |
3 |
126,749,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R4936:Ank2
|
UTSW |
3 |
126,748,688 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4937:Ank2
|
UTSW |
3 |
126,756,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R4946:Ank2
|
UTSW |
3 |
126,735,589 (GRCm39) |
intron |
probably benign |
|
R4963:Ank2
|
UTSW |
3 |
126,825,745 (GRCm39) |
missense |
probably benign |
0.01 |
R4989:Ank2
|
UTSW |
3 |
126,757,094 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5023:Ank2
|
UTSW |
3 |
126,735,520 (GRCm39) |
intron |
probably benign |
|
R5060:Ank2
|
UTSW |
3 |
126,739,570 (GRCm39) |
intron |
probably benign |
|
R5078:Ank2
|
UTSW |
3 |
126,736,002 (GRCm39) |
intron |
probably benign |
|
R5086:Ank2
|
UTSW |
3 |
126,740,997 (GRCm39) |
intron |
probably benign |
|
R5134:Ank2
|
UTSW |
3 |
126,757,094 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5148:Ank2
|
UTSW |
3 |
126,819,285 (GRCm39) |
splice site |
probably null |
|
R5175:Ank2
|
UTSW |
3 |
126,797,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5275:Ank2
|
UTSW |
3 |
126,825,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R5295:Ank2
|
UTSW |
3 |
126,825,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Ank2
|
UTSW |
3 |
126,739,453 (GRCm39) |
intron |
probably benign |
|
R5309:Ank2
|
UTSW |
3 |
126,753,417 (GRCm39) |
missense |
probably damaging |
0.99 |
R5312:Ank2
|
UTSW |
3 |
126,753,417 (GRCm39) |
missense |
probably damaging |
0.99 |
R5352:Ank2
|
UTSW |
3 |
127,292,640 (GRCm39) |
utr 5 prime |
probably benign |
|
R5355:Ank2
|
UTSW |
3 |
126,737,698 (GRCm39) |
intron |
probably benign |
|
R5386:Ank2
|
UTSW |
3 |
126,775,582 (GRCm39) |
missense |
probably benign |
0.01 |
R5396:Ank2
|
UTSW |
3 |
126,746,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R5518:Ank2
|
UTSW |
3 |
126,753,348 (GRCm39) |
missense |
probably damaging |
0.98 |
R5534:Ank2
|
UTSW |
3 |
126,740,947 (GRCm39) |
intron |
probably benign |
|
R5554:Ank2
|
UTSW |
3 |
126,792,622 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5582:Ank2
|
UTSW |
3 |
126,739,954 (GRCm39) |
intron |
probably benign |
|
R5747:Ank2
|
UTSW |
3 |
126,735,400 (GRCm39) |
intron |
probably benign |
|
R5794:Ank2
|
UTSW |
3 |
126,723,669 (GRCm39) |
missense |
probably benign |
0.00 |
R5831:Ank2
|
UTSW |
3 |
127,132,808 (GRCm39) |
start gained |
probably benign |
|
R5925:Ank2
|
UTSW |
3 |
126,726,612 (GRCm39) |
missense |
probably benign |
0.18 |
R5954:Ank2
|
UTSW |
3 |
126,791,510 (GRCm39) |
missense |
probably benign |
0.34 |
R5956:Ank2
|
UTSW |
3 |
126,736,337 (GRCm39) |
intron |
probably benign |
|
R5986:Ank2
|
UTSW |
3 |
126,806,335 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5992:Ank2
|
UTSW |
3 |
126,753,300 (GRCm39) |
critical splice donor site |
probably null |
|
R6020:Ank2
|
UTSW |
3 |
126,740,470 (GRCm39) |
intron |
probably benign |
|
R6027:Ank2
|
UTSW |
3 |
126,791,528 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6049:Ank2
|
UTSW |
3 |
126,736,669 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6060:Ank2
|
UTSW |
3 |
126,749,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R6114:Ank2
|
UTSW |
3 |
126,804,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R6124:Ank2
|
UTSW |
3 |
127,041,800 (GRCm39) |
missense |
probably benign |
0.31 |
R6156:Ank2
|
UTSW |
3 |
126,737,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R6173:Ank2
|
UTSW |
3 |
126,846,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R6176:Ank2
|
UTSW |
3 |
126,739,120 (GRCm39) |
missense |
probably benign |
0.05 |
R6184:Ank2
|
UTSW |
3 |
126,756,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R6199:Ank2
|
UTSW |
3 |
126,797,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R6241:Ank2
|
UTSW |
3 |
126,846,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R6254:Ank2
|
UTSW |
3 |
126,735,453 (GRCm39) |
intron |
probably benign |
|
R6259:Ank2
|
UTSW |
3 |
126,810,635 (GRCm39) |
missense |
probably benign |
0.28 |
R6260:Ank2
|
UTSW |
3 |
126,737,206 (GRCm39) |
missense |
probably benign |
|
R6321:Ank2
|
UTSW |
3 |
126,740,587 (GRCm39) |
intron |
probably benign |
|
R6393:Ank2
|
UTSW |
3 |
126,723,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6406:Ank2
|
UTSW |
3 |
126,825,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R6544:Ank2
|
UTSW |
3 |
126,726,871 (GRCm39) |
missense |
probably damaging |
0.99 |
R6583:Ank2
|
UTSW |
3 |
126,810,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R6739:Ank2
|
UTSW |
3 |
126,873,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R6754:Ank2
|
UTSW |
3 |
126,890,488 (GRCm39) |
intron |
probably benign |
|
R6786:Ank2
|
UTSW |
3 |
126,752,581 (GRCm39) |
missense |
probably damaging |
0.99 |
R6798:Ank2
|
UTSW |
3 |
126,737,913 (GRCm39) |
intron |
probably benign |
|
R6882:Ank2
|
UTSW |
3 |
126,739,406 (GRCm39) |
intron |
probably benign |
|
R6940:Ank2
|
UTSW |
3 |
126,735,621 (GRCm39) |
intron |
probably benign |
|
R6949:Ank2
|
UTSW |
3 |
126,804,533 (GRCm39) |
missense |
probably benign |
0.00 |
R7001:Ank2
|
UTSW |
3 |
126,871,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Ank2
|
UTSW |
3 |
126,738,499 (GRCm39) |
nonsense |
probably null |
|
R7036:Ank2
|
UTSW |
3 |
126,740,041 (GRCm39) |
intron |
probably benign |
|
R7045:Ank2
|
UTSW |
3 |
126,806,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R7048:Ank2
|
UTSW |
3 |
126,819,267 (GRCm39) |
missense |
probably benign |
0.03 |
R7054:Ank2
|
UTSW |
3 |
126,736,952 (GRCm39) |
intron |
probably benign |
|
R7069:Ank2
|
UTSW |
3 |
126,739,947 (GRCm39) |
intron |
probably benign |
|
R7091:Ank2
|
UTSW |
3 |
126,817,000 (GRCm39) |
missense |
probably damaging |
0.98 |
R7107:Ank2
|
UTSW |
3 |
126,797,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Ank2
|
UTSW |
3 |
126,740,590 (GRCm39) |
missense |
unknown |
|
R7191:Ank2
|
UTSW |
3 |
126,740,041 (GRCm39) |
missense |
unknown |
|
R7272:Ank2
|
UTSW |
3 |
126,736,782 (GRCm39) |
missense |
unknown |
|
R7381:Ank2
|
UTSW |
3 |
126,730,277 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7394:Ank2
|
UTSW |
3 |
126,730,302 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7462:Ank2
|
UTSW |
3 |
126,736,683 (GRCm39) |
missense |
unknown |
|
R7490:Ank2
|
UTSW |
3 |
126,752,538 (GRCm39) |
missense |
probably damaging |
0.99 |
R7514:Ank2
|
UTSW |
3 |
126,819,252 (GRCm39) |
missense |
probably benign |
0.06 |
R7534:Ank2
|
UTSW |
3 |
126,727,982 (GRCm39) |
splice site |
probably null |
|
R7540:Ank2
|
UTSW |
3 |
126,781,808 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7547:Ank2
|
UTSW |
3 |
126,738,852 (GRCm39) |
missense |
unknown |
|
R7579:Ank2
|
UTSW |
3 |
126,740,047 (GRCm39) |
missense |
unknown |
|
R7584:Ank2
|
UTSW |
3 |
126,739,777 (GRCm39) |
nonsense |
probably null |
|
R7625:Ank2
|
UTSW |
3 |
126,846,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7698:Ank2
|
UTSW |
3 |
126,825,860 (GRCm39) |
missense |
probably benign |
0.35 |
R7716:Ank2
|
UTSW |
3 |
126,736,815 (GRCm39) |
missense |
unknown |
|
R7718:Ank2
|
UTSW |
3 |
126,758,662 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7722:Ank2
|
UTSW |
3 |
126,822,951 (GRCm39) |
missense |
probably benign |
0.01 |
R7738:Ank2
|
UTSW |
3 |
126,741,271 (GRCm39) |
missense |
|
|
R7977:Ank2
|
UTSW |
3 |
126,739,356 (GRCm39) |
missense |
unknown |
|
R7987:Ank2
|
UTSW |
3 |
126,739,356 (GRCm39) |
missense |
unknown |
|
R8007:Ank2
|
UTSW |
3 |
126,730,096 (GRCm39) |
intron |
probably benign |
|
R8150:Ank2
|
UTSW |
3 |
126,741,162 (GRCm39) |
missense |
|
|
R8161:Ank2
|
UTSW |
3 |
126,825,778 (GRCm39) |
missense |
|
|
R8196:Ank2
|
UTSW |
3 |
126,723,532 (GRCm39) |
missense |
probably damaging |
0.99 |
R8248:Ank2
|
UTSW |
3 |
126,731,434 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8255:Ank2
|
UTSW |
3 |
126,740,398 (GRCm39) |
missense |
unknown |
|
R8279:Ank2
|
UTSW |
3 |
126,726,820 (GRCm39) |
missense |
probably benign |
0.04 |
R8300:Ank2
|
UTSW |
3 |
126,804,555 (GRCm39) |
missense |
|
|
R8716:Ank2
|
UTSW |
3 |
126,736,488 (GRCm39) |
nonsense |
probably null |
|
R8724:Ank2
|
UTSW |
3 |
126,737,405 (GRCm39) |
missense |
unknown |
|
R8765:Ank2
|
UTSW |
3 |
126,850,731 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8779:Ank2
|
UTSW |
3 |
126,758,751 (GRCm39) |
missense |
probably damaging |
0.99 |
R8783:Ank2
|
UTSW |
3 |
126,846,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R8785:Ank2
|
UTSW |
3 |
126,791,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R8826:Ank2
|
UTSW |
3 |
126,740,951 (GRCm39) |
missense |
unknown |
|
R8872:Ank2
|
UTSW |
3 |
126,791,525 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8903:Ank2
|
UTSW |
3 |
126,840,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Ank2
|
UTSW |
3 |
126,726,720 (GRCm39) |
missense |
probably benign |
0.00 |
R8918:Ank2
|
UTSW |
3 |
126,737,380 (GRCm39) |
missense |
unknown |
|
R8947:Ank2
|
UTSW |
3 |
126,736,396 (GRCm39) |
intron |
probably benign |
|
R8977:Ank2
|
UTSW |
3 |
126,738,575 (GRCm39) |
missense |
unknown |
|
R8990:Ank2
|
UTSW |
3 |
126,841,829 (GRCm39) |
critical splice donor site |
probably null |
|
R8994:Ank2
|
UTSW |
3 |
126,723,471 (GRCm39) |
missense |
probably benign |
0.19 |
R9009:Ank2
|
UTSW |
3 |
126,728,025 (GRCm39) |
unclassified |
probably benign |
|
R9123:Ank2
|
UTSW |
3 |
126,733,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R9125:Ank2
|
UTSW |
3 |
126,733,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R9130:Ank2
|
UTSW |
3 |
126,810,565 (GRCm39) |
missense |
|
|
R9175:Ank2
|
UTSW |
3 |
126,722,402 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9220:Ank2
|
UTSW |
3 |
126,737,086 (GRCm39) |
missense |
unknown |
|
R9225:Ank2
|
UTSW |
3 |
126,736,111 (GRCm39) |
missense |
unknown |
|
R9286:Ank2
|
UTSW |
3 |
126,846,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R9325:Ank2
|
UTSW |
3 |
126,775,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R9367:Ank2
|
UTSW |
3 |
126,738,678 (GRCm39) |
missense |
unknown |
|
R9385:Ank2
|
UTSW |
3 |
126,753,366 (GRCm39) |
missense |
probably benign |
0.00 |
R9391:Ank2
|
UTSW |
3 |
126,731,394 (GRCm39) |
missense |
probably damaging |
0.99 |
R9422:Ank2
|
UTSW |
3 |
126,890,505 (GRCm39) |
missense |
unknown |
|
R9536:Ank2
|
UTSW |
3 |
126,736,031 (GRCm39) |
missense |
unknown |
|
R9647:Ank2
|
UTSW |
3 |
126,792,623 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9650:Ank2
|
UTSW |
3 |
126,735,829 (GRCm39) |
missense |
unknown |
|
R9666:Ank2
|
UTSW |
3 |
126,726,838 (GRCm39) |
nonsense |
probably null |
|
R9686:Ank2
|
UTSW |
3 |
126,740,550 (GRCm39) |
missense |
unknown |
|
R9730:Ank2
|
UTSW |
3 |
127,019,493 (GRCm39) |
missense |
|
|
R9738:Ank2
|
UTSW |
3 |
126,737,121 (GRCm39) |
missense |
unknown |
|
R9743:Ank2
|
UTSW |
3 |
126,733,794 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9747:Ank2
|
UTSW |
3 |
126,752,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R9800:Ank2
|
UTSW |
3 |
126,740,149 (GRCm39) |
missense |
unknown |
|
R9803:Ank2
|
UTSW |
3 |
126,752,726 (GRCm39) |
missense |
possibly damaging |
0.64 |
RF020:Ank2
|
UTSW |
3 |
126,739,125 (GRCm39) |
missense |
unknown |
|
Z1088:Ank2
|
UTSW |
3 |
126,823,158 (GRCm39) |
missense |
possibly damaging |
0.45 |
Z1177:Ank2
|
UTSW |
3 |
126,738,006 (GRCm39) |
missense |
unknown |
|
Z1187:Ank2
|
UTSW |
3 |
126,749,601 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1190:Ank2
|
UTSW |
3 |
126,749,601 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1192:Ank2
|
UTSW |
3 |
126,749,601 (GRCm39) |
missense |
probably damaging |
1.00 |
|