| Other mutations in this stock |
Total: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca7 |
A |
T |
10: 79,844,889 (GRCm39) |
H1537L |
probably damaging |
Het |
| Actg2 |
T |
A |
6: 83,500,169 (GRCm39) |
N116I |
probably damaging |
Het |
| Actn1 |
G |
A |
12: 80,219,796 (GRCm39) |
H692Y |
probably damaging |
Het |
| Adamts6 |
C |
T |
13: 104,449,285 (GRCm39) |
P36S |
probably benign |
Het |
| Agr3 |
G |
A |
12: 35,997,858 (GRCm39) |
|
probably null |
Het |
| BC051019 |
T |
A |
7: 109,317,269 (GRCm39) |
D141V |
probably damaging |
Het |
| Bco1 |
T |
C |
8: 117,835,454 (GRCm39) |
F135S |
probably damaging |
Het |
| Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
| Ccdc42 |
A |
G |
11: 68,485,115 (GRCm39) |
K210E |
probably damaging |
Het |
| Cckar |
A |
T |
5: 53,857,409 (GRCm39) |
W263R |
probably damaging |
Het |
| Cela2a |
A |
G |
4: 141,553,252 (GRCm39) |
|
probably null |
Het |
| Cep97 |
A |
T |
16: 55,748,159 (GRCm39) |
N90K |
probably damaging |
Het |
| Ces2g |
A |
T |
8: 105,693,984 (GRCm39) |
Q440L |
probably damaging |
Het |
| Chchd6 |
G |
T |
6: 89,396,736 (GRCm39) |
T225K |
possibly damaging |
Het |
| Chd1l |
C |
T |
3: 97,490,047 (GRCm39) |
E503K |
probably benign |
Het |
| Chrna5 |
A |
G |
9: 54,911,649 (GRCm39) |
T46A |
probably benign |
Het |
| Col16a1 |
G |
A |
4: 129,992,733 (GRCm39) |
G1531S |
probably damaging |
Het |
| Col19a1 |
A |
T |
1: 24,573,172 (GRCm39) |
V200E |
unknown |
Het |
| Csf2rb |
A |
G |
15: 78,219,411 (GRCm39) |
D2G |
probably damaging |
Het |
| Csmd3 |
G |
A |
15: 47,813,346 (GRCm39) |
S1062L |
probably damaging |
Het |
| Cul5 |
G |
T |
9: 53,569,893 (GRCm39) |
Q113K |
probably benign |
Het |
| Dmwd |
TAGCCTGGGAA |
TAGCCTGGGAAGCCTGGGAA |
7: 18,814,959 (GRCm39) |
|
probably benign |
Het |
| Dse |
T |
C |
10: 34,029,230 (GRCm39) |
D620G |
probably damaging |
Het |
| Dsg1c |
A |
G |
18: 20,397,899 (GRCm39) |
N33S |
probably benign |
Het |
| Epc2 |
G |
A |
2: 49,439,990 (GRCm39) |
V803I |
probably damaging |
Het |
| Erap1 |
T |
A |
13: 74,819,500 (GRCm39) |
H171Q |
probably damaging |
Het |
| Esrrb |
T |
C |
12: 86,561,274 (GRCm39) |
V336A |
possibly damaging |
Het |
| Fech |
A |
T |
18: 64,595,189 (GRCm39) |
W300R |
probably damaging |
Het |
| Fgd4 |
T |
C |
16: 16,241,920 (GRCm39) |
I635V |
possibly damaging |
Het |
| Galc |
A |
T |
12: 98,200,563 (GRCm39) |
N282K |
probably benign |
Het |
| Gpat2 |
A |
G |
2: 127,270,637 (GRCm39) |
Y95C |
probably benign |
Het |
| Grm2 |
T |
A |
9: 106,524,670 (GRCm39) |
I682F |
probably damaging |
Het |
| Hdac10 |
G |
T |
15: 89,010,878 (GRCm39) |
A241D |
probably damaging |
Het |
| Helz |
T |
A |
11: 107,527,105 (GRCm39) |
C182* |
probably null |
Het |
| Ift140 |
A |
G |
17: 25,307,839 (GRCm39) |
Y978C |
probably damaging |
Het |
| Intu |
T |
A |
3: 40,652,061 (GRCm39) |
C839* |
probably null |
Het |
| Jmjd1c |
T |
C |
10: 67,055,654 (GRCm39) |
V358A |
probably benign |
Het |
| Kif26b |
A |
G |
1: 178,744,043 (GRCm39) |
S1380G |
probably benign |
Het |
| Lrp1b |
A |
G |
2: 40,587,601 (GRCm39) |
S116P |
unknown |
Het |
| Lrrc2 |
T |
A |
9: 110,790,041 (GRCm39) |
S99R |
probably benign |
Het |
| Mrpl48 |
G |
A |
7: 100,195,482 (GRCm39) |
|
probably benign |
Het |
| Mup9 |
A |
G |
4: 60,377,878 (GRCm39) |
|
probably benign |
Het |
| Nap1l1 |
G |
A |
10: 111,329,240 (GRCm39) |
V285I |
possibly damaging |
Het |
| Nepro |
A |
G |
16: 44,547,391 (GRCm39) |
D36G |
probably benign |
Het |
| Nkain4 |
A |
G |
2: 180,577,794 (GRCm39) |
F187L |
probably damaging |
Het |
| Nobox |
A |
T |
6: 43,284,401 (GRCm39) |
C82S |
possibly damaging |
Het |
| Ntn4 |
C |
A |
10: 93,480,596 (GRCm39) |
Q70K |
probably damaging |
Het |
| Or13j1 |
A |
G |
4: 43,706,292 (GRCm39) |
I92T |
probably damaging |
Het |
| Or1e26 |
A |
T |
11: 73,480,118 (GRCm39) |
W149R |
probably damaging |
Het |
| Or4k37 |
A |
G |
2: 111,159,306 (GRCm39) |
I181V |
probably benign |
Het |
| Or51a43 |
T |
C |
7: 103,717,738 (GRCm39) |
R167G |
probably damaging |
Het |
| Or5b122 |
T |
A |
19: 13,562,978 (GRCm39) |
F103L |
probably benign |
Het |
| Or9r3 |
A |
G |
10: 129,948,548 (GRCm39) |
I37T |
possibly damaging |
Het |
| Pappa |
A |
G |
4: 65,094,466 (GRCm39) |
E497G |
probably damaging |
Het |
| Pard3 |
C |
A |
8: 128,106,983 (GRCm39) |
T569K |
probably benign |
Het |
| Parp14 |
G |
A |
16: 35,677,130 (GRCm39) |
A946V |
probably benign |
Het |
| Pcdh10 |
A |
G |
3: 45,334,747 (GRCm39) |
N354D |
possibly damaging |
Het |
| Pdgfc |
T |
C |
3: 81,082,194 (GRCm39) |
V129A |
probably benign |
Het |
| Pdia3 |
G |
A |
2: 121,262,858 (GRCm39) |
G275S |
probably damaging |
Het |
| Phf20l1 |
A |
T |
15: 66,487,108 (GRCm39) |
H407L |
possibly damaging |
Het |
| Phip |
A |
T |
9: 82,753,502 (GRCm39) |
D1747E |
probably benign |
Het |
| Pkd1l1 |
A |
G |
11: 8,900,413 (GRCm39) |
S43P |
probably damaging |
Het |
| Plekhg2 |
T |
C |
7: 28,067,846 (GRCm39) |
E202G |
probably damaging |
Het |
| Rapsn |
A |
G |
2: 90,873,504 (GRCm39) |
D270G |
possibly damaging |
Het |
| Rims2 |
A |
C |
15: 39,370,382 (GRCm39) |
S939R |
probably damaging |
Het |
| Ripor3 |
T |
C |
2: 167,822,765 (GRCm39) |
D932G |
probably damaging |
Het |
| Rtp2 |
A |
T |
16: 23,749,421 (GRCm39) |
W30R |
probably damaging |
Het |
| Scgb2b27 |
A |
T |
7: 33,711,557 (GRCm39) |
D97E |
probably benign |
Het |
| Slc25a46 |
T |
C |
18: 31,716,542 (GRCm39) |
N320S |
probably benign |
Het |
| Slc9b1 |
A |
G |
3: 135,060,765 (GRCm39) |
|
probably null |
Het |
| Socs4 |
T |
A |
14: 47,527,740 (GRCm39) |
M225K |
possibly damaging |
Het |
| Spata31d1a |
A |
T |
13: 59,850,247 (GRCm39) |
L627* |
probably null |
Het |
| Srcin1 |
A |
G |
11: 97,416,307 (GRCm39) |
L975P |
probably damaging |
Het |
| Stard3 |
T |
A |
11: 98,267,435 (GRCm39) |
|
probably null |
Het |
| Susd2 |
G |
T |
10: 75,473,878 (GRCm39) |
S572R |
possibly damaging |
Het |
| Tll1 |
C |
A |
8: 64,509,307 (GRCm39) |
A568S |
probably benign |
Het |
| Tmem132a |
C |
G |
19: 10,839,062 (GRCm39) |
G460A |
probably damaging |
Het |
| Trim62 |
A |
G |
4: 128,803,281 (GRCm39) |
K444E |
probably damaging |
Het |
| Trpm3 |
A |
G |
19: 22,689,271 (GRCm39) |
T67A |
probably damaging |
Het |
| Ttc6 |
T |
C |
12: 57,784,454 (GRCm39) |
M1841T |
possibly damaging |
Het |
| Ulk2 |
A |
T |
11: 61,672,572 (GRCm39) |
V922D |
probably damaging |
Het |
| Vmn2r38 |
C |
A |
7: 9,078,532 (GRCm39) |
V617L |
probably damaging |
Het |
| Xkr6 |
G |
A |
14: 64,056,766 (GRCm39) |
V226M |
probably benign |
Het |
| Zfp940 |
G |
A |
7: 29,544,962 (GRCm39) |
A315V |
possibly damaging |
Het |
| Zfr |
C |
A |
15: 12,150,473 (GRCm39) |
T480K |
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 |
|
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 |
|
R1986:Ank3
|
UTSW |
10 |
69,703,258 (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