Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ace3 |
A |
G |
11: 105,888,364 (GRCm39) |
D358G |
probably damaging |
Het |
Actmap |
T |
C |
7: 26,900,503 (GRCm39) |
S161P |
probably benign |
Het |
Adgrd1 |
G |
A |
5: 129,174,138 (GRCm39) |
|
probably benign |
Het |
Aff4 |
C |
A |
11: 53,271,444 (GRCm39) |
T327K |
probably damaging |
Het |
Ajap1 |
A |
G |
4: 153,470,961 (GRCm39) |
V282A |
probably damaging |
Het |
Arrb1 |
A |
G |
7: 99,240,568 (GRCm39) |
D194G |
probably benign |
Het |
Atp1a3 |
T |
C |
7: 24,680,979 (GRCm39) |
N836S |
probably damaging |
Het |
C1ql3 |
A |
G |
2: 13,015,567 (GRCm39) |
V31A |
probably benign |
Het |
Cc2d2a |
A |
G |
5: 43,896,692 (GRCm39) |
T1530A |
probably damaging |
Het |
Cenpc1 |
A |
T |
5: 86,164,209 (GRCm39) |
I804K |
probably damaging |
Het |
Chmp2b |
G |
A |
16: 65,359,422 (GRCm39) |
|
probably benign |
Het |
Chrm5 |
T |
A |
2: 112,310,453 (GRCm39) |
E221V |
possibly damaging |
Het |
Col22a1 |
A |
T |
15: 71,878,796 (GRCm39) |
H120Q |
probably damaging |
Het |
Esp16 |
C |
T |
17: 39,850,729 (GRCm39) |
A36V |
probably damaging |
Het |
Fn1 |
A |
T |
1: 71,682,308 (GRCm39) |
S283T |
probably benign |
Het |
Hipk3 |
A |
G |
2: 104,264,179 (GRCm39) |
L773S |
probably damaging |
Het |
Lcor |
C |
T |
19: 41,573,698 (GRCm39) |
R818W |
probably damaging |
Het |
Morn3 |
A |
G |
5: 123,175,825 (GRCm39) |
W188R |
probably damaging |
Het |
Msantd2 |
T |
G |
9: 37,434,798 (GRCm39) |
L547R |
probably damaging |
Het |
Naip5 |
T |
A |
13: 100,356,338 (GRCm39) |
E1092D |
probably benign |
Het |
Obi1 |
A |
T |
14: 104,717,082 (GRCm39) |
C430* |
probably null |
Het |
Or4a15 |
A |
T |
2: 89,193,652 (GRCm39) |
N40K |
probably damaging |
Het |
Or7e166 |
T |
C |
9: 19,624,653 (GRCm39) |
F177L |
possibly damaging |
Het |
Pcdhga5 |
G |
A |
18: 37,828,826 (GRCm39) |
V425I |
probably benign |
Het |
Pdxk |
T |
A |
10: 78,283,786 (GRCm39) |
Y136F |
probably benign |
Het |
Prr14 |
T |
C |
7: 127,075,410 (GRCm39) |
F503L |
probably benign |
Het |
Prss54 |
T |
C |
8: 96,286,057 (GRCm39) |
I339V |
probably benign |
Het |
Repin1 |
T |
C |
6: 48,574,073 (GRCm39) |
I334T |
probably damaging |
Het |
Runx3 |
A |
G |
4: 134,882,720 (GRCm39) |
D152G |
probably damaging |
Het |
She |
T |
A |
3: 89,739,256 (GRCm39) |
I149N |
probably damaging |
Het |
Stra6 |
A |
G |
9: 58,042,254 (GRCm39) |
|
probably benign |
Het |
Syvn1 |
A |
G |
19: 6,100,393 (GRCm39) |
D288G |
probably damaging |
Het |
Tacc1 |
T |
C |
8: 25,672,077 (GRCm39) |
S384G |
probably benign |
Het |
Tmc8 |
ACTTCCT |
ACT |
11: 117,681,558 (GRCm39) |
|
probably null |
Het |
Trhr |
T |
C |
15: 44,061,149 (GRCm39) |
I223T |
possibly damaging |
Het |
Vmn2r45 |
A |
G |
7: 8,484,371 (GRCm39) |
I478T |
possibly damaging |
Het |
Zbtb3 |
G |
T |
19: 8,781,173 (GRCm39) |
R262M |
possibly damaging |
Het |
Zfp516 |
T |
C |
18: 83,006,080 (GRCm39) |
S995P |
probably benign |
Het |
Zfp985 |
A |
G |
4: 147,668,412 (GRCm39) |
I427V |
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 |
R4969:Svil
|
UTSW |
18 |
5,095,516 (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 |
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 |
|