Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
G |
T |
11: 110,087,865 (GRCm39) |
N1087K |
probably benign |
Het |
Abcc3 |
G |
A |
11: 94,250,438 (GRCm39) |
T921I |
probably benign |
Het |
Abr |
T |
A |
11: 76,399,812 (GRCm39) |
I4F |
probably damaging |
Het |
Adcy10 |
T |
A |
1: 165,330,812 (GRCm39) |
V25D |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,983,231 (GRCm39) |
M1505K |
probably damaging |
Het |
Alms1-ps2 |
T |
C |
6: 85,773,231 (GRCm39) |
|
noncoding transcript |
Het |
Apob |
C |
G |
12: 8,061,559 (GRCm39) |
T3347S |
probably damaging |
Het |
Arhgap27 |
C |
A |
11: 103,230,822 (GRCm39) |
G11W |
probably damaging |
Het |
Ccdc110 |
A |
T |
8: 46,393,605 (GRCm39) |
I106F |
probably damaging |
Het |
Ccdc28b |
T |
A |
4: 129,514,806 (GRCm39) |
D101V |
probably damaging |
Het |
Ccdc30 |
T |
C |
4: 119,188,324 (GRCm39) |
E566G |
probably benign |
Het |
Cenpm |
T |
C |
15: 82,123,565 (GRCm39) |
S111G |
probably benign |
Het |
Cep55 |
A |
G |
19: 38,046,348 (GRCm39) |
I34V |
probably benign |
Het |
Dcdc2a |
T |
C |
13: 25,291,585 (GRCm39) |
L190S |
probably damaging |
Het |
Dhh |
T |
C |
15: 98,792,441 (GRCm39) |
|
probably null |
Het |
Dst |
A |
G |
1: 34,203,200 (GRCm39) |
N703S |
probably null |
Het |
E030025P04Rik |
G |
A |
11: 109,030,396 (GRCm39) |
L164F |
unknown |
Het |
Efcab5 |
A |
G |
11: 77,025,701 (GRCm39) |
V538A |
probably benign |
Het |
Egflam |
A |
G |
15: 7,333,422 (GRCm39) |
S177P |
probably benign |
Het |
Ehbp1l1 |
A |
T |
19: 5,775,958 (GRCm39) |
C31S |
probably damaging |
Het |
Eif2d |
C |
A |
1: 131,098,797 (GRCm39) |
Q532K |
probably damaging |
Het |
Elf3 |
T |
C |
1: 135,184,531 (GRCm39) |
D175G |
possibly damaging |
Het |
F5 |
T |
C |
1: 164,012,129 (GRCm39) |
V449A |
probably damaging |
Het |
Fam110a |
A |
T |
2: 151,811,954 (GRCm39) |
I272N |
probably damaging |
Het |
Fbxo34 |
A |
G |
14: 47,768,464 (GRCm39) |
D608G |
probably damaging |
Het |
Flrt2 |
T |
C |
12: 95,746,058 (GRCm39) |
L132P |
probably damaging |
Het |
Frg2f1 |
A |
T |
4: 119,388,277 (GRCm39) |
V74D |
possibly damaging |
Het |
Gad1 |
G |
T |
2: 70,404,597 (GRCm39) |
E162D |
probably benign |
Het |
Glb1l |
A |
G |
1: 75,177,104 (GRCm39) |
V444A |
probably damaging |
Het |
Gm10770 |
G |
A |
2: 150,021,076 (GRCm39) |
T147I |
probably damaging |
Het |
Gm43302 |
T |
C |
5: 105,425,602 (GRCm39) |
I276V |
probably benign |
Het |
Greb1 |
T |
C |
12: 16,746,244 (GRCm39) |
H1314R |
probably damaging |
Het |
Hapln2 |
A |
G |
3: 87,931,308 (GRCm39) |
V69A |
probably damaging |
Het |
Hcn1 |
T |
C |
13: 118,112,544 (GRCm39) |
I836T |
probably damaging |
Het |
Hspa5 |
A |
G |
2: 34,665,815 (GRCm39) |
D553G |
probably damaging |
Het |
Iqgap1 |
A |
T |
7: 80,410,631 (GRCm39) |
I194N |
probably damaging |
Het |
Kansl3 |
A |
G |
1: 36,390,825 (GRCm39) |
V304A |
probably damaging |
Het |
Kdm5d |
C |
T |
Y: 927,798 (GRCm39) |
S716L |
probably damaging |
Het |
Klra6 |
T |
C |
6: 129,999,573 (GRCm39) |
T132A |
probably benign |
Het |
Krt26 |
CTAGTA |
CTA |
11: 99,224,352 (GRCm39) |
|
probably benign |
Het |
Lrp1 |
A |
G |
10: 127,409,337 (GRCm39) |
I1594T |
possibly damaging |
Het |
Lrp2bp |
A |
G |
8: 46,464,152 (GRCm39) |
D15G |
probably benign |
Het |
Map4k1 |
T |
C |
7: 28,686,588 (GRCm39) |
L170P |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,233,037 (GRCm39) |
F1108L |
possibly damaging |
Het |
Mettl5 |
G |
T |
2: 69,715,686 (GRCm39) |
L6I |
unknown |
Het |
Mfsd14a |
A |
T |
3: 116,426,057 (GRCm39) |
F447I |
possibly damaging |
Het |
Mrc2 |
A |
G |
11: 105,228,546 (GRCm39) |
I642V |
probably damaging |
Het |
Necap1 |
A |
G |
6: 122,851,547 (GRCm39) |
Y7C |
probably damaging |
Het |
Nsd1 |
G |
A |
13: 55,394,258 (GRCm39) |
E723K |
probably damaging |
Het |
Nsun3 |
A |
T |
16: 62,596,755 (GRCm39) |
L121H |
probably damaging |
Het |
Nsun6 |
A |
T |
2: 15,014,288 (GRCm39) |
M284K |
probably damaging |
Het |
Nutf2 |
T |
C |
8: 106,603,242 (GRCm39) |
|
probably null |
Het |
Odad2 |
A |
T |
18: 7,223,551 (GRCm39) |
D497E |
probably benign |
Het |
Or1j20 |
A |
T |
2: 36,759,601 (GRCm39) |
N8Y |
probably damaging |
Het |
Or5d38 |
A |
T |
2: 87,954,471 (GRCm39) |
M286K |
probably damaging |
Het |
Pacs1 |
T |
C |
19: 5,205,912 (GRCm39) |
E288G |
probably damaging |
Het |
Peg10 |
A |
T |
6: 4,756,381 (GRCm39) |
|
probably benign |
Het |
Rab38 |
G |
A |
7: 88,099,730 (GRCm39) |
E82K |
possibly damaging |
Het |
Rgsl1 |
T |
A |
1: 153,675,543 (GRCm39) |
E206V |
probably damaging |
Het |
Saxo5 |
T |
A |
8: 3,533,668 (GRCm39) |
F295L |
possibly damaging |
Het |
Scube3 |
G |
A |
17: 28,384,063 (GRCm39) |
V521I |
probably damaging |
Het |
Sgpp1 |
C |
T |
12: 75,762,982 (GRCm39) |
V400M |
probably damaging |
Het |
Slc18b1 |
T |
C |
10: 23,681,891 (GRCm39) |
S152P |
possibly damaging |
Het |
Slit1 |
A |
T |
19: 41,709,477 (GRCm39) |
|
probably null |
Het |
Spata31d1e |
T |
C |
13: 59,890,320 (GRCm39) |
Y82C |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,023,513 (GRCm39) |
K640R |
probably benign |
Het |
Timm44 |
A |
G |
8: 4,310,510 (GRCm39) |
|
probably null |
Het |
Tomm40 |
A |
G |
7: 19,447,650 (GRCm39) |
S127P |
probably benign |
Het |
Vmn2r23 |
T |
A |
6: 123,706,649 (GRCm39) |
V493D |
possibly damaging |
Het |
Yeats2 |
T |
C |
16: 19,989,988 (GRCm39) |
V288A |
probably damaging |
Het |
Zfhx4 |
C |
T |
3: 5,466,558 (GRCm39) |
R2239W |
probably damaging |
Het |
Zscan2 |
A |
C |
7: 80,525,301 (GRCm39) |
K341Q |
probably 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 |
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 |
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 |
|