Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
A |
G |
7: 45,754,943 (GRCm39) |
I1525T |
probably benign |
Het |
Agtpbp1 |
A |
G |
13: 59,648,392 (GRCm39) |
V476A |
probably benign |
Het |
Aipl1 |
A |
G |
11: 71,922,256 (GRCm39) |
I151T |
probably benign |
Het |
Apc |
C |
T |
18: 34,445,971 (GRCm39) |
R938* |
probably null |
Het |
Atp2a2 |
A |
G |
5: 122,596,554 (GRCm39) |
F855S |
possibly damaging |
Het |
Axdnd1 |
T |
C |
1: 156,223,075 (GRCm39) |
T261A |
possibly damaging |
Het |
Cbfa2t2 |
A |
G |
2: 154,365,900 (GRCm39) |
D370G |
probably damaging |
Het |
Cep350 |
T |
C |
1: 155,736,025 (GRCm39) |
I2964V |
probably damaging |
Het |
Clec16a |
T |
C |
16: 10,386,375 (GRCm39) |
V158A |
probably damaging |
Het |
Col6a5 |
G |
A |
9: 105,741,806 (GRCm39) |
T2371I |
probably damaging |
Het |
Cpne8 |
T |
C |
15: 90,503,929 (GRCm39) |
T79A |
probably damaging |
Het |
Cyp2b13 |
A |
G |
7: 25,780,413 (GRCm39) |
R145G |
probably damaging |
Het |
Disc1 |
G |
A |
8: 125,851,289 (GRCm39) |
W391* |
probably null |
Het |
Dnah8 |
G |
A |
17: 30,941,988 (GRCm39) |
V1745I |
probably damaging |
Het |
Dsp |
T |
C |
13: 38,376,886 (GRCm39) |
V1557A |
probably benign |
Het |
Egfem1 |
T |
A |
3: 29,637,145 (GRCm39) |
Y194N |
probably damaging |
Het |
Eif4a3 |
A |
G |
11: 119,179,705 (GRCm39) |
Y361H |
probably damaging |
Het |
Esd |
T |
A |
14: 74,982,153 (GRCm39) |
S189R |
possibly damaging |
Het |
Fancf |
A |
T |
7: 51,511,196 (GRCm39) |
Y269* |
probably null |
Het |
Fbln2 |
A |
T |
6: 91,248,569 (GRCm39) |
H1078L |
possibly damaging |
Het |
Fbxw13 |
A |
G |
9: 109,010,592 (GRCm39) |
|
probably null |
Het |
Fcgr2b |
A |
T |
1: 170,790,941 (GRCm39) |
V284D |
probably benign |
Het |
Fuz |
G |
A |
7: 44,549,718 (GRCm39) |
G363R |
probably damaging |
Het |
Gas7 |
A |
G |
11: 67,574,234 (GRCm39) |
E403G |
probably damaging |
Het |
Gnl1 |
A |
G |
17: 36,291,581 (GRCm39) |
D49G |
possibly damaging |
Het |
Gucy2g |
A |
G |
19: 55,214,445 (GRCm39) |
V561A |
probably benign |
Het |
H1f7 |
A |
T |
15: 98,154,216 (GRCm39) |
V311E |
unknown |
Het |
Hebp2 |
T |
C |
10: 18,420,122 (GRCm39) |
T104A |
probably benign |
Het |
Ighv1-19 |
T |
A |
12: 114,672,377 (GRCm39) |
Q80L |
probably benign |
Het |
Kctd19 |
T |
A |
8: 106,122,959 (GRCm39) |
|
probably null |
Het |
Kdm3b |
T |
C |
18: 34,955,428 (GRCm39) |
L905P |
probably damaging |
Het |
Klkb1 |
T |
C |
8: 45,735,814 (GRCm39) |
D183G |
probably benign |
Het |
Krt6b |
T |
C |
15: 101,588,460 (GRCm39) |
R67G |
possibly damaging |
Het |
Krt75 |
T |
C |
15: 101,482,248 (GRCm39) |
I7V |
probably benign |
Het |
Lpo |
A |
T |
11: 87,697,751 (GRCm39) |
N685K |
probably benign |
Het |
Mroh7 |
A |
T |
4: 106,538,070 (GRCm39) |
I1202N |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,754,572 (GRCm38) |
M1482K |
probably benign |
Het |
Mylk |
T |
A |
16: 34,791,810 (GRCm39) |
V1494E |
probably damaging |
Het |
Neurl4 |
A |
G |
11: 69,801,913 (GRCm39) |
D17G |
probably damaging |
Het |
Nkx6-3 |
A |
G |
8: 23,647,725 (GRCm39) |
Y228C |
probably damaging |
Het |
Nprl2 |
G |
A |
9: 107,420,273 (GRCm39) |
|
probably null |
Het |
Nxf1 |
A |
G |
19: 8,739,669 (GRCm39) |
|
probably null |
Het |
Or4a39 |
A |
G |
2: 89,236,770 (GRCm39) |
F218L |
probably benign |
Het |
Or52u1 |
A |
T |
7: 104,237,730 (GRCm39) |
N240Y |
probably damaging |
Het |
Pde3b |
A |
G |
7: 114,118,847 (GRCm39) |
E662G |
possibly damaging |
Het |
Plekhm3 |
G |
A |
1: 64,977,078 (GRCm39) |
R131C |
probably damaging |
Het |
Plpp7 |
T |
C |
2: 31,985,950 (GRCm39) |
S43P |
probably benign |
Het |
Pramel5 |
A |
G |
4: 143,998,187 (GRCm39) |
L352P |
probably damaging |
Het |
Prepl |
T |
C |
17: 85,395,902 (GRCm39) |
S27G |
probably benign |
Het |
Ptprd |
A |
G |
4: 76,051,542 (GRCm39) |
I227T |
probably damaging |
Het |
Pttg1ip |
C |
T |
10: 77,419,854 (GRCm39) |
Q6* |
probably null |
Het |
Rgl1 |
C |
T |
1: 152,424,813 (GRCm39) |
|
probably null |
Het |
Riiad1 |
C |
A |
3: 94,380,173 (GRCm39) |
G41* |
probably null |
Het |
Rnf214 |
C |
T |
9: 45,807,486 (GRCm39) |
R239H |
probably damaging |
Het |
Rpap3 |
C |
T |
15: 97,584,407 (GRCm39) |
V346I |
probably benign |
Het |
Scaf4 |
G |
A |
16: 90,048,831 (GRCm39) |
Q328* |
probably null |
Het |
Sec23a |
A |
G |
12: 59,051,274 (GRCm39) |
|
probably null |
Het |
Slc5a8 |
T |
A |
10: 88,740,774 (GRCm39) |
|
probably null |
Het |
Slc9a8 |
A |
G |
2: 167,288,449 (GRCm39) |
T183A |
probably benign |
Het |
Sod3 |
A |
T |
5: 52,525,736 (GRCm39) |
H145L |
probably damaging |
Het |
Sp4 |
A |
G |
12: 118,263,341 (GRCm39) |
V235A |
probably damaging |
Het |
Spp1 |
A |
C |
5: 104,588,153 (GRCm39) |
E185A |
possibly damaging |
Het |
Susd1 |
A |
T |
4: 59,351,679 (GRCm39) |
W461R |
probably benign |
Het |
Tdrd12 |
A |
T |
7: 35,186,720 (GRCm39) |
|
probably null |
Het |
Terb1 |
A |
T |
8: 105,221,795 (GRCm39) |
N168K |
probably benign |
Het |
Tnnt1 |
A |
G |
7: 4,510,573 (GRCm39) |
L216P |
probably damaging |
Het |
Ttc28 |
A |
G |
5: 111,424,121 (GRCm39) |
K1463E |
probably damaging |
Het |
Twf2 |
T |
G |
9: 106,089,098 (GRCm39) |
|
probably null |
Het |
Urb1 |
C |
T |
16: 90,602,299 (GRCm39) |
R90Q |
probably damaging |
Het |
Wdr45b |
A |
T |
11: 121,219,650 (GRCm39) |
C299* |
probably null |
Het |
Wrap73 |
A |
G |
4: 154,237,138 (GRCm39) |
S54G |
probably damaging |
Het |
Zeb2 |
T |
C |
2: 44,888,931 (GRCm39) |
K323R |
probably damaging |
Het |
Zfp410 |
T |
C |
12: 84,378,582 (GRCm39) |
I302T |
possibly damaging |
Het |
|
Other mutations in Svil |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Svil
|
APN |
18 |
5,099,045 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00840:Svil
|
APN |
18 |
5,063,555 (GRCm39) |
missense |
probably benign |
|
IGL01329:Svil
|
APN |
18 |
5,064,501 (GRCm39) |
missense |
probably benign |
|
IGL01446:Svil
|
APN |
18 |
5,062,385 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02068:Svil
|
APN |
18 |
5,092,899 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02223:Svil
|
APN |
18 |
5,105,879 (GRCm39) |
splice site |
probably benign |
|
IGL02428:Svil
|
APN |
18 |
5,118,203 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02429:Svil
|
APN |
18 |
5,118,369 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02479:Svil
|
APN |
18 |
5,099,476 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02560:Svil
|
APN |
18 |
5,049,379 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02652:Svil
|
APN |
18 |
5,114,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03291:Svil
|
APN |
18 |
5,056,150 (GRCm39) |
nonsense |
probably null |
|
R3779_Svil_985
|
UTSW |
18 |
5,090,855 (GRCm39) |
missense |
probably damaging |
0.97 |
R5433_Svil_176
|
UTSW |
18 |
5,059,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R6062_Svil_873
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
BB002:Svil
|
UTSW |
18 |
5,118,357 (GRCm39) |
missense |
probably benign |
0.00 |
BB012:Svil
|
UTSW |
18 |
5,118,357 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03055:Svil
|
UTSW |
18 |
5,108,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R0029:Svil
|
UTSW |
18 |
5,063,286 (GRCm39) |
missense |
probably benign |
0.14 |
R0029:Svil
|
UTSW |
18 |
5,063,286 (GRCm39) |
missense |
probably benign |
0.14 |
R0266:Svil
|
UTSW |
18 |
5,099,063 (GRCm39) |
splice site |
probably benign |
|
R0281:Svil
|
UTSW |
18 |
5,094,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Svil
|
UTSW |
18 |
5,046,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R0549:Svil
|
UTSW |
18 |
5,064,566 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0617:Svil
|
UTSW |
18 |
5,117,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R0801:Svil
|
UTSW |
18 |
5,099,443 (GRCm39) |
missense |
probably benign |
0.00 |
R0894:Svil
|
UTSW |
18 |
5,097,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R1053:Svil
|
UTSW |
18 |
5,056,690 (GRCm39) |
missense |
probably benign |
0.16 |
R1065:Svil
|
UTSW |
18 |
5,063,777 (GRCm39) |
splice site |
probably benign |
|
R1080:Svil
|
UTSW |
18 |
5,058,147 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1199:Svil
|
UTSW |
18 |
5,059,217 (GRCm39) |
splice site |
probably benign |
|
R1472:Svil
|
UTSW |
18 |
5,048,950 (GRCm39) |
missense |
probably benign |
0.09 |
R1480:Svil
|
UTSW |
18 |
5,057,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Svil
|
UTSW |
18 |
5,046,817 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1626:Svil
|
UTSW |
18 |
5,117,099 (GRCm39) |
critical splice donor site |
probably null |
|
R1691:Svil
|
UTSW |
18 |
5,056,336 (GRCm39) |
missense |
probably benign |
0.06 |
R1812:Svil
|
UTSW |
18 |
5,097,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Svil
|
UTSW |
18 |
5,063,383 (GRCm39) |
missense |
probably benign |
0.01 |
R1842:Svil
|
UTSW |
18 |
5,062,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Svil
|
UTSW |
18 |
5,094,640 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1945:Svil
|
UTSW |
18 |
5,117,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R2184:Svil
|
UTSW |
18 |
5,099,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R2184:Svil
|
UTSW |
18 |
5,099,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Svil
|
UTSW |
18 |
5,046,640 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R2398:Svil
|
UTSW |
18 |
5,060,613 (GRCm39) |
splice site |
probably null |
|
R3076:Svil
|
UTSW |
18 |
5,116,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R3777:Svil
|
UTSW |
18 |
5,090,855 (GRCm39) |
missense |
probably damaging |
0.97 |
R3779:Svil
|
UTSW |
18 |
5,090,855 (GRCm39) |
missense |
probably damaging |
0.97 |
R3797:Svil
|
UTSW |
18 |
5,060,534 (GRCm39) |
missense |
probably benign |
0.29 |
R4077:Svil
|
UTSW |
18 |
5,063,522 (GRCm39) |
missense |
probably benign |
0.03 |
R4350:Svil
|
UTSW |
18 |
5,118,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Svil
|
UTSW |
18 |
5,046,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R4488:Svil
|
UTSW |
18 |
5,049,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Svil
|
UTSW |
18 |
5,088,813 (GRCm39) |
missense |
probably damaging |
0.99 |
R4825:Svil
|
UTSW |
18 |
5,114,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Svil
|
UTSW |
18 |
5,108,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Svil
|
UTSW |
18 |
5,054,025 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4990:Svil
|
UTSW |
18 |
5,056,810 (GRCm39) |
missense |
probably benign |
0.05 |
R4991:Svil
|
UTSW |
18 |
5,056,810 (GRCm39) |
missense |
probably benign |
0.05 |
R5061:Svil
|
UTSW |
18 |
5,048,954 (GRCm39) |
missense |
probably benign |
0.02 |
R5271:Svil
|
UTSW |
18 |
5,062,329 (GRCm39) |
missense |
probably benign |
0.45 |
R5362:Svil
|
UTSW |
18 |
5,057,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R5433:Svil
|
UTSW |
18 |
5,059,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R5677:Svil
|
UTSW |
18 |
5,046,823 (GRCm39) |
nonsense |
probably null |
|
R5850:Svil
|
UTSW |
18 |
5,098,900 (GRCm39) |
splice site |
probably null |
|
R5868:Svil
|
UTSW |
18 |
5,056,854 (GRCm39) |
splice site |
probably null |
|
R5871:Svil
|
UTSW |
18 |
5,103,669 (GRCm39) |
splice site |
probably null |
|
R5876:Svil
|
UTSW |
18 |
5,082,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6061:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6065:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6066:Svil
|
UTSW |
18 |
5,106,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6114:Svil
|
UTSW |
18 |
5,108,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6115:Svil
|
UTSW |
18 |
5,108,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R6117:Svil
|
UTSW |
18 |
5,116,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Svil
|
UTSW |
18 |
5,057,432 (GRCm39) |
missense |
probably benign |
0.13 |
R6418:Svil
|
UTSW |
18 |
5,040,171 (GRCm39) |
missense |
probably benign |
0.26 |
R6441:Svil
|
UTSW |
18 |
5,049,323 (GRCm39) |
missense |
probably benign |
|
R6446:Svil
|
UTSW |
18 |
5,057,323 (GRCm39) |
missense |
probably benign |
0.09 |
R6455:Svil
|
UTSW |
18 |
5,056,629 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6545:Svil
|
UTSW |
18 |
5,108,621 (GRCm39) |
missense |
probably benign |
0.00 |
R6692:Svil
|
UTSW |
18 |
5,082,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R6730:Svil
|
UTSW |
18 |
5,049,311 (GRCm39) |
missense |
probably benign |
0.17 |
R6763:Svil
|
UTSW |
18 |
5,056,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R6870:Svil
|
UTSW |
18 |
5,063,231 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6916:Svil
|
UTSW |
18 |
5,114,682 (GRCm39) |
utr 3 prime |
probably benign |
|
R7134:Svil
|
UTSW |
18 |
5,116,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Svil
|
UTSW |
18 |
5,092,937 (GRCm39) |
missense |
probably benign |
0.01 |
R7213:Svil
|
UTSW |
18 |
5,094,574 (GRCm39) |
missense |
probably damaging |
0.99 |
R7249:Svil
|
UTSW |
18 |
5,062,247 (GRCm39) |
missense |
probably damaging |
0.99 |
R7249:Svil
|
UTSW |
18 |
5,056,270 (GRCm39) |
missense |
probably benign |
0.01 |
R7421:Svil
|
UTSW |
18 |
5,056,109 (GRCm39) |
missense |
probably benign |
0.18 |
R7571:Svil
|
UTSW |
18 |
5,114,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Svil
|
UTSW |
18 |
5,095,188 (GRCm39) |
missense |
probably benign |
0.16 |
R7645:Svil
|
UTSW |
18 |
5,099,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R7925:Svil
|
UTSW |
18 |
5,118,357 (GRCm39) |
missense |
probably benign |
0.00 |
R8113:Svil
|
UTSW |
18 |
5,062,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R8263:Svil
|
UTSW |
18 |
5,108,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R8485:Svil
|
UTSW |
18 |
5,064,566 (GRCm39) |
missense |
probably benign |
0.03 |
R8491:Svil
|
UTSW |
18 |
5,106,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R8752:Svil
|
UTSW |
18 |
5,060,366 (GRCm39) |
intron |
probably benign |
|
R8774:Svil
|
UTSW |
18 |
5,049,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774-TAIL:Svil
|
UTSW |
18 |
5,049,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8780:Svil
|
UTSW |
18 |
5,063,449 (GRCm39) |
missense |
probably benign |
0.00 |
R8787:Svil
|
UTSW |
18 |
5,059,332 (GRCm39) |
nonsense |
probably null |
|
R8790:Svil
|
UTSW |
18 |
5,056,098 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8974:Svil
|
UTSW |
18 |
5,099,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R9029:Svil
|
UTSW |
18 |
5,056,239 (GRCm39) |
missense |
probably benign |
|
R9072:Svil
|
UTSW |
18 |
5,097,500 (GRCm39) |
missense |
probably benign |
0.23 |
R9073:Svil
|
UTSW |
18 |
5,097,500 (GRCm39) |
missense |
probably benign |
0.23 |
R9079:Svil
|
UTSW |
18 |
5,056,308 (GRCm39) |
missense |
probably benign |
0.31 |
R9181:Svil
|
UTSW |
18 |
5,090,833 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9363:Svil
|
UTSW |
18 |
5,037,155 (GRCm39) |
missense |
probably benign |
0.02 |
R9377:Svil
|
UTSW |
18 |
5,057,294 (GRCm39) |
missense |
probably benign |
0.06 |
R9381:Svil
|
UTSW |
18 |
5,099,013 (GRCm39) |
missense |
probably benign |
0.06 |
R9389:Svil
|
UTSW |
18 |
5,090,811 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9566:Svil
|
UTSW |
18 |
5,099,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R9607:Svil
|
UTSW |
18 |
5,058,126 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9716:Svil
|
UTSW |
18 |
5,062,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:Svil
|
UTSW |
18 |
5,049,062 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Svil
|
UTSW |
18 |
5,062,317 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Svil
|
UTSW |
18 |
5,062,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|