| Other mutations in this stock |
Total: 91 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700006A11Rik |
A |
G |
3: 124,212,977 (GRCm39) |
S105P |
probably damaging |
Het |
| 9930111J21Rik2 |
T |
A |
11: 48,910,119 (GRCm39) |
K771N |
possibly damaging |
Het |
| Abcc2 |
A |
G |
19: 43,818,318 (GRCm39) |
E1268G |
probably damaging |
Het |
| Adamts4 |
T |
C |
1: 171,084,244 (GRCm39) |
F574L |
possibly damaging |
Het |
| Adamts9 |
A |
G |
6: 92,773,375 (GRCm39) |
V1165A |
probably benign |
Het |
| Agap2 |
A |
T |
10: 126,918,913 (GRCm39) |
K430* |
probably null |
Het |
| Amn |
G |
T |
12: 111,241,431 (GRCm39) |
G232V |
probably damaging |
Het |
| Arhgap45 |
T |
C |
10: 79,856,530 (GRCm39) |
L26P |
probably damaging |
Het |
| Atp10b |
C |
A |
11: 43,063,595 (GRCm39) |
Q177K |
probably benign |
Het |
| Bbs10 |
A |
T |
10: 111,135,118 (GRCm39) |
D77V |
probably damaging |
Het |
| Bltp2 |
A |
T |
11: 78,165,438 (GRCm39) |
H1318L |
probably damaging |
Het |
| Bpifa1 |
T |
A |
2: 153,986,256 (GRCm39) |
L127Q |
probably damaging |
Het |
| Brinp2 |
T |
C |
1: 158,074,348 (GRCm39) |
N591S |
probably damaging |
Het |
| C2cd2 |
A |
C |
16: 97,671,471 (GRCm39) |
V476G |
probably damaging |
Het |
| C7 |
T |
A |
15: 5,041,494 (GRCm39) |
T471S |
possibly damaging |
Het |
| Cacna1b |
A |
T |
2: 24,538,998 (GRCm39) |
Y1488N |
probably damaging |
Het |
| Cadps2 |
A |
G |
6: 23,323,379 (GRCm39) |
F1001L |
probably damaging |
Het |
| Ccdc188 |
T |
C |
16: 18,036,707 (GRCm39) |
S216P |
probably damaging |
Het |
| Ccdc24 |
A |
G |
4: 117,729,213 (GRCm39) |
L88P |
probably damaging |
Het |
| Dab1 |
T |
C |
4: 104,470,412 (GRCm39) |
I65T |
probably damaging |
Het |
| Dock4 |
A |
T |
12: 40,780,062 (GRCm39) |
D621V |
probably damaging |
Het |
| Drd5 |
A |
T |
5: 38,477,456 (GRCm39) |
M150L |
probably damaging |
Het |
| Eef2k |
T |
A |
7: 120,472,569 (GRCm39) |
M94K |
possibly damaging |
Het |
| Epg5 |
A |
G |
18: 78,025,521 (GRCm39) |
|
probably null |
Het |
| Epsti1 |
T |
C |
14: 78,169,673 (GRCm39) |
|
probably null |
Het |
| Ern2 |
T |
A |
7: 121,770,752 (GRCm39) |
D754V |
probably benign |
Het |
| Fbxo6 |
A |
G |
4: 148,230,552 (GRCm39) |
Y237H |
probably damaging |
Het |
| Fbxw24 |
A |
G |
9: 109,436,124 (GRCm39) |
S303P |
probably damaging |
Het |
| Fpr-rs3 |
A |
T |
17: 20,844,103 (GRCm39) |
|
probably null |
Het |
| Gab1 |
G |
T |
8: 81,493,010 (GRCm39) |
T679K |
probably damaging |
Het |
| Gbp9 |
C |
A |
5: 105,253,590 (GRCm39) |
V42F |
probably damaging |
Het |
| Gbp9 |
A |
T |
5: 105,253,652 (GRCm39) |
V21E |
probably damaging |
Het |
| Gm20821 |
A |
G |
Y: 9,783,927 (GRCm39) |
Q183R |
probably benign |
Het |
| Gpatch11 |
A |
T |
17: 79,151,266 (GRCm39) |
I226F |
probably benign |
Het |
| Hephl1 |
T |
G |
9: 14,965,848 (GRCm39) |
E1035A |
probably damaging |
Het |
| Hspa4l |
T |
C |
3: 40,714,833 (GRCm39) |
V156A |
probably damaging |
Het |
| Ifna13 |
A |
G |
4: 88,562,588 (GRCm39) |
V12A |
probably benign |
Het |
| Il24 |
G |
A |
1: 130,810,268 (GRCm39) |
T196I |
probably benign |
Het |
| Irgm2 |
A |
G |
11: 58,110,384 (GRCm39) |
D37G |
probably benign |
Het |
| Irs1 |
A |
G |
1: 82,266,486 (GRCm39) |
S577P |
probably damaging |
Het |
| Kif21b |
G |
A |
1: 136,075,284 (GRCm39) |
D166N |
probably damaging |
Het |
| Krtap4-16 |
T |
C |
11: 99,742,322 (GRCm39) |
Q26R |
unknown |
Het |
| Lig1 |
T |
A |
7: 13,043,067 (GRCm39) |
Y837* |
probably null |
Het |
| Lrrc69 |
T |
C |
4: 14,708,669 (GRCm39) |
E225G |
possibly damaging |
Het |
| Map3k20 |
C |
T |
2: 72,271,638 (GRCm39) |
Q589* |
probably null |
Het |
| Masp1 |
T |
G |
16: 23,302,211 (GRCm39) |
M347L |
probably benign |
Het |
| Mgat3 |
A |
T |
15: 80,096,390 (GRCm39) |
I406F |
probably benign |
Het |
| Mmp1b |
T |
G |
9: 7,368,577 (GRCm39) |
D425A |
probably benign |
Het |
| Mss51 |
T |
C |
14: 20,533,259 (GRCm39) |
H404R |
probably benign |
Het |
| Myo15b |
A |
T |
11: 115,773,701 (GRCm39) |
H1911L |
probably benign |
Het |
| Nedd4l |
A |
G |
18: 65,276,874 (GRCm39) |
D102G |
probably damaging |
Het |
| Niban3 |
T |
A |
8: 72,056,404 (GRCm39) |
I368N |
possibly damaging |
Het |
| Npc2 |
T |
C |
12: 84,807,523 (GRCm39) |
K112E |
probably benign |
Het |
| Nuggc |
T |
A |
14: 65,879,370 (GRCm39) |
V694E |
probably damaging |
Het |
| Olfm1 |
T |
G |
2: 28,104,718 (GRCm39) |
V157G |
probably benign |
Het |
| Or10h28 |
T |
C |
17: 33,488,489 (GRCm39) |
S264P |
probably benign |
Het |
| Or5p55 |
T |
C |
7: 107,566,877 (GRCm39) |
V91A |
probably benign |
Het |
| Otogl |
T |
A |
10: 107,630,051 (GRCm39) |
|
probably null |
Het |
| Ovgp1 |
G |
A |
3: 105,882,251 (GRCm39) |
C38Y |
probably damaging |
Het |
| Pisd |
A |
T |
5: 32,894,672 (GRCm39) |
S344T |
probably damaging |
Het |
| Psme4 |
T |
C |
11: 30,780,352 (GRCm39) |
V840A |
probably benign |
Het |
| Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
| Rims2 |
T |
A |
15: 39,208,710 (GRCm39) |
M171K |
probably damaging |
Het |
| Rin2 |
T |
A |
2: 145,720,860 (GRCm39) |
M731K |
probably damaging |
Het |
| Scgb1b19 |
T |
C |
7: 32,987,108 (GRCm39) |
|
probably null |
Het |
| Serpina10 |
A |
G |
12: 103,594,514 (GRCm39) |
I235T |
possibly damaging |
Het |
| Setbp1 |
T |
A |
18: 78,901,759 (GRCm39) |
E636V |
probably damaging |
Het |
| Sh3d21 |
C |
T |
4: 126,056,290 (GRCm39) |
E101K |
probably damaging |
Het |
| Ski |
T |
G |
4: 155,306,148 (GRCm39) |
D225A |
probably damaging |
Het |
| Slc28a2b |
A |
G |
2: 122,357,910 (GRCm39) |
T655A |
probably benign |
Het |
| Slc29a3 |
T |
C |
10: 60,559,593 (GRCm39) |
Y187C |
probably damaging |
Het |
| Sort1 |
T |
A |
3: 108,253,043 (GRCm39) |
D494E |
possibly damaging |
Het |
| Sphkap |
A |
T |
1: 83,255,643 (GRCm39) |
L702Q |
probably damaging |
Het |
| Srr |
A |
G |
11: 74,799,545 (GRCm39) |
I285T |
probably damaging |
Het |
| Stam2 |
T |
C |
2: 52,599,638 (GRCm39) |
T257A |
possibly damaging |
Het |
| Suds3 |
A |
T |
5: 117,246,417 (GRCm39) |
N112K |
probably damaging |
Het |
| Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
| Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
| Tesk2 |
T |
C |
4: 116,608,390 (GRCm39) |
L104P |
probably damaging |
Het |
| Tie1 |
C |
T |
4: 118,336,160 (GRCm39) |
R702H |
probably benign |
Het |
| Tpo |
G |
T |
12: 30,169,465 (GRCm39) |
A90E |
probably damaging |
Het |
| Trim30a |
T |
C |
7: 104,060,672 (GRCm39) |
D368G |
probably damaging |
Het |
| Ugt2a2 |
A |
T |
5: 87,608,438 (GRCm39) |
M633K |
possibly damaging |
Het |
| Vars2 |
A |
G |
17: 35,970,953 (GRCm39) |
W626R |
probably damaging |
Het |
| Vmn2r10 |
A |
T |
5: 109,154,120 (GRCm39) |
Y61* |
probably null |
Het |
| Vmn2r95 |
T |
C |
17: 18,671,805 (GRCm39) |
V514A |
probably benign |
Het |
| Vwa5a |
T |
G |
9: 38,649,110 (GRCm39) |
|
probably benign |
Het |
| Zfp365 |
A |
T |
10: 67,745,686 (GRCm39) |
C31S |
probably damaging |
Het |
| Zfp397 |
A |
T |
18: 24,093,108 (GRCm39) |
I198F |
possibly damaging |
Het |
| Zfp407 |
C |
T |
18: 84,577,898 (GRCm39) |
A1072T |
probably benign |
Het |
| Zfp593 |
T |
C |
4: 133,972,206 (GRCm39) |
E100G |
possibly damaging |
Het |
|
| Other mutations in Ank3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00514:Ank3
|
APN |
10 |
69,818,035 (GRCm39) |
splice site |
probably benign |
|
|
IGL00578:Ank3
|
APN |
10 |
69,838,224 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL00851:Ank3
|
APN |
10 |
69,710,663 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01067:Ank3
|
APN |
10 |
69,686,026 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01483:Ank3
|
APN |
10 |
69,710,639 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01549:Ank3
|
APN |
10 |
69,768,250 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01576:Ank3
|
APN |
10 |
69,816,121 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01601:Ank3
|
APN |
10 |
69,840,555 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL02047:Ank3
|
APN |
10 |
69,728,324 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL02088:Ank3
|
APN |
10 |
69,835,203 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02159:Ank3
|
APN |
10 |
69,644,722 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02249:Ank3
|
APN |
10 |
69,718,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02942:Ank3
|
APN |
10 |
69,809,707 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02979:Ank3
|
APN |
10 |
69,837,929 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03379:Ank3
|
APN |
10 |
69,809,602 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4495001:Ank3
|
UTSW |
10 |
69,828,902 (GRCm39) |
missense |
|
|
|
R0011:Ank3
|
UTSW |
10 |
69,815,281 (GRCm39) |
splice site |
probably benign |
|
|
R0011:Ank3
|
UTSW |
10 |
69,815,281 (GRCm39) |
splice site |
probably benign |
|
|
R0172:Ank3
|
UTSW |
10 |
69,811,888 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0315:Ank3
|
UTSW |
10 |
69,838,347 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0480:Ank3
|
UTSW |
10 |
69,715,756 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0485:Ank3
|
UTSW |
10 |
69,718,374 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R0511:Ank3
|
UTSW |
10 |
69,718,198 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1148:Ank3
|
UTSW |
10 |
69,718,369 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1148:Ank3
|
UTSW |
10 |
69,718,369 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1165:Ank3
|
UTSW |
10 |
69,734,132 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1186:Ank3
|
UTSW |
10 |
69,703,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1257:Ank3
|
UTSW |
10 |
69,710,665 (GRCm39) |
nonsense |
probably null |
|
|
R1300:Ank3
|
UTSW |
10 |
69,840,495 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1391:Ank3
|
UTSW |
10 |
69,370,110 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R1549:Ank3
|
UTSW |
10 |
69,837,812 (GRCm39) |
missense |
probably benign |
0.18 |
|
R1586:Ank3
|
UTSW |
10 |
69,713,708 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1619:Ank3
|
UTSW |
10 |
69,715,805 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1643:Ank3
|
UTSW |
10 |
69,720,632 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1874:Ank3
|
UTSW |
10 |
69,733,913 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1884:Ank3
|
UTSW |
10 |
69,851,422 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1901:Ank3
|
UTSW |
10 |
69,658,167 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2051:Ank3
|
UTSW |
10 |
69,733,920 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R2273:Ank3
|
UTSW |
10 |
69,786,772 (GRCm39) |
splice site |
probably null |
|
|
R2274:Ank3
|
UTSW |
10 |
69,786,772 (GRCm39) |
splice site |
probably null |
|
|
R2421:Ank3
|
UTSW |
10 |
69,818,034 (GRCm39) |
splice site |
probably benign |
|
|
R2434:Ank3
|
UTSW |
10 |
69,837,948 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2969:Ank3
|
UTSW |
10 |
69,830,225 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3426:Ank3
|
UTSW |
10 |
69,542,724 (GRCm39) |
missense |
probably benign |
|
|
R3885:Ank3
|
UTSW |
10 |
69,734,866 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3936:Ank3
|
UTSW |
10 |
69,715,819 (GRCm39) |
nonsense |
probably null |
|
|
R4258:Ank3
|
UTSW |
10 |
69,840,592 (GRCm39) |
missense |
probably benign |
0.33 |
|
R4320:Ank3
|
UTSW |
10 |
69,740,076 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R4434:Ank3
|
UTSW |
10 |
69,822,900 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4435:Ank3
|
UTSW |
10 |
69,822,900 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4486:Ank3
|
UTSW |
10 |
69,837,804 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R4489:Ank3
|
UTSW |
10 |
69,734,086 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4492:Ank3
|
UTSW |
10 |
69,644,755 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4508:Ank3
|
UTSW |
10 |
69,728,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4561:Ank3
|
UTSW |
10 |
69,837,848 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4724:Ank3
|
UTSW |
10 |
69,542,688 (GRCm39) |
missense |
probably benign |
|
|
R4751:Ank3
|
UTSW |
10 |
69,822,036 (GRCm39) |
missense |
probably benign |
0.19 |
|
R4790:Ank3
|
UTSW |
10 |
69,823,981 (GRCm39) |
nonsense |
probably null |
|
|
R4795:Ank3
|
UTSW |
10 |
69,694,095 (GRCm39) |
missense |
probably benign |
0.36 |
|
R4921:Ank3
|
UTSW |
10 |
69,837,939 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4932:Ank3
|
UTSW |
10 |
69,734,053 (GRCm39) |
splice site |
probably null |
|
|
R4935:Ank3
|
UTSW |
10 |
69,812,033 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4946:Ank3
|
UTSW |
10 |
69,733,947 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5174:Ank3
|
UTSW |
10 |
69,728,209 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5208:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5248:Ank3
|
UTSW |
10 |
69,822,938 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5255:Ank3
|
UTSW |
10 |
69,721,030 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5307:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5308:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5373:Ank3
|
UTSW |
10 |
69,789,306 (GRCm39) |
splice site |
probably null |
|
|
R5374:Ank3
|
UTSW |
10 |
69,789,306 (GRCm39) |
splice site |
probably null |
|
|
R5502:Ank3
|
UTSW |
10 |
69,756,291 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5508:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5509:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5510:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5538:Ank3
|
UTSW |
10 |
69,823,257 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5664:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5665:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5682:Ank3
|
UTSW |
10 |
69,729,347 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5834:Ank3
|
UTSW |
10 |
69,658,087 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5881:Ank3
|
UTSW |
10 |
69,822,660 (GRCm39) |
missense |
probably benign |
0.31 |
|
R5914:Ank3
|
UTSW |
10 |
69,828,774 (GRCm39) |
intron |
probably benign |
|
|
R5940:Ank3
|
UTSW |
10 |
69,756,316 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5952:Ank3
|
UTSW |
10 |
69,822,293 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5963:Ank3
|
UTSW |
10 |
69,823,056 (GRCm39) |
nonsense |
probably null |
|
|
R6075:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6076:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6077:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6081:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6092:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6118:Ank3
|
UTSW |
10 |
69,830,231 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6135:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6175:Ank3
|
UTSW |
10 |
69,763,557 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6248:Ank3
|
UTSW |
10 |
69,809,680 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6249:Ank3
|
UTSW |
10 |
69,658,906 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R6273:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6274:Ank3
|
UTSW |
10 |
69,838,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6290:Ank3
|
UTSW |
10 |
69,827,198 (GRCm39) |
intron |
probably benign |
|
|
R6298:Ank3
|
UTSW |
10 |
69,686,006 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6349:Ank3
|
UTSW |
10 |
69,815,269 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6366:Ank3
|
UTSW |
10 |
69,835,188 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6371:Ank3
|
UTSW |
10 |
69,644,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6459:Ank3
|
UTSW |
10 |
69,827,577 (GRCm39) |
intron |
probably benign |
|
|
R6489:Ank3
|
UTSW |
10 |
69,827,459 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6491:Ank3
|
UTSW |
10 |
69,827,459 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6499:Ank3
|
UTSW |
10 |
69,827,574 (GRCm39) |
intron |
probably benign |
|
|
R6520:Ank3
|
UTSW |
10 |
69,824,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6521:Ank3
|
UTSW |
10 |
69,828,596 (GRCm39) |
intron |
probably benign |
|
|
R6535:Ank3
|
UTSW |
10 |
69,713,684 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6548:Ank3
|
UTSW |
10 |
69,728,240 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6587:Ank3
|
UTSW |
10 |
69,825,982 (GRCm39) |
intron |
probably benign |
|
|
R6624:Ank3
|
UTSW |
10 |
69,740,298 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R6722:Ank3
|
UTSW |
10 |
69,826,074 (GRCm39) |
intron |
probably benign |
|
|
R6729:Ank3
|
UTSW |
10 |
69,644,755 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6731:Ank3
|
UTSW |
10 |
69,849,858 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R6742:Ank3
|
UTSW |
10 |
69,827,412 (GRCm39) |
intron |
probably benign |
|
|
R6788:Ank3
|
UTSW |
10 |
69,840,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6846:Ank3
|
UTSW |
10 |
69,660,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6933:Ank3
|
UTSW |
10 |
69,740,042 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7034:Ank3
|
UTSW |
10 |
69,835,209 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7036:Ank3
|
UTSW |
10 |
69,835,209 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7132:Ank3
|
UTSW |
10 |
69,825,744 (GRCm39) |
missense |
|
|
|
R7171:Ank3
|
UTSW |
10 |
69,828,311 (GRCm39) |
missense |
|
|
|
R7241:Ank3
|
UTSW |
10 |
69,542,644 (GRCm39) |
start codon destroyed |
probably null |
0.11 |
|
R7386:Ank3
|
UTSW |
10 |
69,658,079 (GRCm39) |
missense |
unknown |
|
|
R7445:Ank3
|
UTSW |
10 |
69,827,954 (GRCm39) |
missense |
|
|
|
R7452:Ank3
|
UTSW |
10 |
69,734,881 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R7492:Ank3
|
UTSW |
10 |
69,718,357 (GRCm39) |
missense |
unknown |
|
|
R7494:Ank3
|
UTSW |
10 |
69,824,756 (GRCm39) |
missense |
|
|
|
R7512:Ank3
|
UTSW |
10 |
69,826,691 (GRCm39) |
missense |
|
|
|
R7543:Ank3
|
UTSW |
10 |
69,786,846 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R7577:Ank3
|
UTSW |
10 |
69,828,402 (GRCm39) |
missense |
|
|
|
R7610:Ank3
|
UTSW |
10 |
69,822,252 (GRCm39) |
missense |
|
|
|
R7673:Ank3
|
UTSW |
10 |
69,826,331 (GRCm39) |
missense |
|
|
|
R7682:Ank3
|
UTSW |
10 |
69,824,065 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R7814:Ank3
|
UTSW |
10 |
69,822,734 (GRCm39) |
missense |
|
|
|
R7835:Ank3
|
UTSW |
10 |
69,823,557 (GRCm39) |
missense |
|
|
|
R7843:Ank3
|
UTSW |
10 |
69,822,788 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7891:Ank3
|
UTSW |
10 |
69,824,139 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8109:Ank3
|
UTSW |
10 |
69,826,148 (GRCm39) |
missense |
|
|
|
R8175:Ank3
|
UTSW |
10 |
69,729,339 (GRCm39) |
missense |
unknown |
|
|
R8210:Ank3
|
UTSW |
10 |
69,811,925 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R8211:Ank3
|
UTSW |
10 |
69,703,228 (GRCm39) |
missense |
unknown |
|
|
R8299:Ank3
|
UTSW |
10 |
69,811,981 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8302:Ank3
|
UTSW |
10 |
69,840,810 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R8516:Ank3
|
UTSW |
10 |
69,763,559 (GRCm39) |
nonsense |
probably null |
|
|
R8543:Ank3
|
UTSW |
10 |
69,838,266 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8549:Ank3
|
UTSW |
10 |
69,818,012 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R8726:Ank3
|
UTSW |
10 |
69,823,084 (GRCm39) |
missense |
|
|
|
R8729:Ank3
|
UTSW |
10 |
69,838,428 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R8735:Ank3
|
UTSW |
10 |
69,822,785 (GRCm39) |
missense |
probably benign |
0.24 |
|
R8751:Ank3
|
UTSW |
10 |
69,761,849 (GRCm39) |
intron |
probably benign |
|
|
R8788:Ank3
|
UTSW |
10 |
69,718,256 (GRCm39) |
missense |
unknown |
|
|
R8875:Ank3
|
UTSW |
10 |
69,660,233 (GRCm39) |
missense |
unknown |
|
|
R8919:Ank3
|
UTSW |
10 |
69,840,671 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R8932:Ank3
|
UTSW |
10 |
69,660,292 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9053:Ank3
|
UTSW |
10 |
69,822,389 (GRCm39) |
missense |
|
|
|
R9064:Ank3
|
UTSW |
10 |
69,822,185 (GRCm39) |
missense |
|
|
|
R9084:Ank3
|
UTSW |
10 |
69,786,879 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9160:Ank3
|
UTSW |
10 |
69,838,304 (GRCm39) |
missense |
unknown |
|
|
R9275:Ank3
|
UTSW |
10 |
69,822,662 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9280:Ank3
|
UTSW |
10 |
69,818,021 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9300:Ank3
|
UTSW |
10 |
69,706,872 (GRCm39) |
missense |
unknown |
|
|
R9302:Ank3
|
UTSW |
10 |
69,761,849 (GRCm39) |
intron |
probably benign |
|
|
R9327:Ank3
|
UTSW |
10 |
69,812,086 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9336:Ank3
|
UTSW |
10 |
69,809,578 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9345:Ank3
|
UTSW |
10 |
69,761,899 (GRCm39) |
intron |
probably benign |
|
|
R9368:Ank3
|
UTSW |
10 |
69,823,329 (GRCm39) |
missense |
|
|
|
R9406:Ank3
|
UTSW |
10 |
69,645,011 (GRCm39) |
missense |
unknown |
|
|
R9491:Ank3
|
UTSW |
10 |
69,838,339 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R9573:Ank3
|
UTSW |
10 |
69,791,977 (GRCm39) |
nonsense |
probably null |
|
|
R9674:Ank3
|
UTSW |
10 |
69,824,549 (GRCm39) |
missense |
|
|
|
R9710:Ank3
|
UTSW |
10 |
69,829,070 (GRCm39) |
missense |
|
|
|
R9720:Ank3
|
UTSW |
10 |
69,825,335 (GRCm39) |
missense |
|
|
|
R9767:Ank3
|
UTSW |
10 |
69,823,799 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9800:Ank3
|
UTSW |
10 |
69,733,957 (GRCm39) |
missense |
unknown |
|
|
Z1176:Ank3
|
UTSW |
10 |
69,827,045 (GRCm39) |
missense |
|
|
|
Z1176:Ank3
|
UTSW |
10 |
69,786,840 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
Z1176:Ank3
|
UTSW |
10 |
69,768,304 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
Incidental Mutation