Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
C |
T |
4: 62,450,578 (GRCm39) |
R51W |
probably damaging |
Het |
Abcb1a |
T |
A |
5: 8,752,920 (GRCm39) |
L557Q |
probably damaging |
Het |
Abcb4 |
T |
C |
5: 8,968,662 (GRCm39) |
F334L |
possibly damaging |
Het |
Adamts14 |
T |
A |
10: 61,034,583 (GRCm39) |
T1102S |
probably benign |
Het |
Adamtsl1 |
T |
C |
4: 86,344,102 (GRCm39) |
Y1719H |
probably damaging |
Het |
Adcyap1 |
T |
C |
17: 93,507,550 (GRCm39) |
|
probably null |
Het |
Ankrd13c |
T |
A |
3: 157,677,947 (GRCm39) |
L219Q |
probably damaging |
Het |
Ano3 |
C |
A |
2: 110,711,174 (GRCm39) |
A97S |
probably benign |
Het |
Apaf1 |
T |
C |
10: 90,898,022 (GRCm39) |
N245S |
probably benign |
Het |
Apob |
A |
G |
12: 8,056,047 (GRCm39) |
T1510A |
probably benign |
Het |
Apob |
A |
G |
12: 8,061,937 (GRCm39) |
D3473G |
possibly damaging |
Het |
Arfgap3 |
G |
A |
15: 83,191,138 (GRCm39) |
T12I |
probably benign |
Het |
Bend4 |
A |
G |
5: 67,557,418 (GRCm39) |
V466A |
probably damaging |
Het |
Bend7 |
G |
A |
2: 4,749,239 (GRCm39) |
E119K |
probably damaging |
Het |
Capn5 |
G |
T |
7: 97,781,049 (GRCm39) |
R243S |
possibly damaging |
Het |
Cd84 |
A |
G |
1: 171,679,510 (GRCm39) |
I63V |
probably benign |
Het |
Cd86 |
T |
A |
16: 36,449,350 (GRCm39) |
T16S |
probably benign |
Het |
Cdc42bpb |
A |
G |
12: 111,262,734 (GRCm39) |
|
probably benign |
Het |
Cep20 |
G |
A |
16: 14,122,380 (GRCm39) |
T128I |
possibly damaging |
Het |
Cep95 |
C |
T |
11: 106,708,781 (GRCm39) |
S26L |
probably damaging |
Het |
Cldn19 |
C |
T |
4: 119,112,810 (GRCm39) |
A14V |
probably damaging |
Het |
Cluap1 |
T |
A |
16: 3,755,453 (GRCm39) |
M356K |
probably damaging |
Het |
Coq7 |
C |
T |
7: 118,109,260 (GRCm39) |
G263S |
unknown |
Het |
Ctnnd2 |
A |
C |
15: 30,847,445 (GRCm39) |
T679P |
probably damaging |
Het |
Dnah10 |
A |
G |
5: 124,820,750 (GRCm39) |
D528G |
possibly damaging |
Het |
Dvl1 |
T |
A |
4: 155,938,476 (GRCm39) |
N133K |
probably damaging |
Het |
Efcab7 |
T |
G |
4: 99,769,744 (GRCm39) |
H550Q |
probably null |
Het |
Fastkd5 |
C |
T |
2: 130,456,717 (GRCm39) |
M624I |
probably damaging |
Het |
Fbxo42 |
T |
C |
4: 140,895,073 (GRCm39) |
V12A |
probably benign |
Het |
Gabarapl1 |
T |
A |
6: 129,515,635 (GRCm39) |
M91K |
possibly damaging |
Het |
Gas7 |
A |
G |
11: 67,552,902 (GRCm39) |
N154S |
probably damaging |
Het |
Gm21814 |
T |
A |
6: 149,483,650 (GRCm39) |
|
noncoding transcript |
Het |
Gnl3 |
G |
A |
14: 30,739,803 (GRCm39) |
R12C |
probably damaging |
Het |
Golga2 |
T |
G |
2: 32,187,807 (GRCm39) |
|
probably null |
Het |
Grk3 |
T |
A |
5: 113,062,878 (GRCm39) |
R656S |
probably benign |
Het |
Gsap |
T |
A |
5: 21,412,236 (GRCm39) |
|
probably benign |
Het |
H60c |
T |
C |
10: 3,210,240 (GRCm39) |
Q103R |
probably benign |
Het |
Hnrnpr |
T |
A |
4: 136,056,755 (GRCm39) |
S252T |
probably damaging |
Het |
Krtap27-1 |
T |
C |
16: 88,468,302 (GRCm39) |
N81D |
probably benign |
Het |
Lilrb4a |
T |
A |
10: 51,367,683 (GRCm39) |
L75Q |
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,313,738 (GRCm39) |
D2331V |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,290,821 (GRCm39) |
E3546D |
probably damaging |
Het |
Lzts2 |
T |
A |
19: 45,009,893 (GRCm39) |
V9E |
probably damaging |
Het |
Matr3 |
T |
A |
18: 35,717,709 (GRCm39) |
D302E |
probably benign |
Het |
Mcoln2 |
A |
G |
3: 145,897,979 (GRCm39) |
|
probably null |
Het |
Metap2 |
T |
C |
10: 93,704,811 (GRCm39) |
D272G |
probably damaging |
Het |
Mitf |
A |
G |
6: 97,987,428 (GRCm39) |
D337G |
probably damaging |
Het |
Mrtfb |
T |
C |
16: 13,219,433 (GRCm39) |
V693A |
possibly damaging |
Het |
Msh2 |
A |
G |
17: 87,985,771 (GRCm39) |
E116G |
probably benign |
Het |
Nlrp10 |
T |
A |
7: 108,523,555 (GRCm39) |
M642L |
probably benign |
Het |
Noxa1 |
G |
T |
2: 24,982,558 (GRCm39) |
Q86K |
probably benign |
Het |
Nrap |
T |
C |
19: 56,372,562 (GRCm39) |
T48A |
probably benign |
Het |
Nup160 |
T |
A |
2: 90,520,494 (GRCm39) |
H308Q |
probably damaging |
Het |
Osbpl11 |
T |
C |
16: 33,056,699 (GRCm39) |
L711P |
probably damaging |
Het |
Osbpl6 |
A |
G |
2: 76,385,409 (GRCm39) |
N281S |
probably benign |
Het |
Pcnp |
C |
T |
16: 55,844,703 (GRCm39) |
E66K |
possibly damaging |
Het |
Phf11 |
T |
A |
14: 59,482,227 (GRCm39) |
E175D |
probably damaging |
Het |
Pik3cg |
A |
G |
12: 32,254,983 (GRCm39) |
Y335H |
probably damaging |
Het |
Plekhg4 |
T |
C |
8: 106,108,431 (GRCm39) |
L1053S |
probably damaging |
Het |
Plekhh2 |
G |
T |
17: 84,918,203 (GRCm39) |
E1271* |
probably null |
Het |
Ppp2r2b |
T |
A |
18: 42,871,055 (GRCm39) |
Y82F |
probably damaging |
Het |
Prkd3 |
T |
C |
17: 79,278,796 (GRCm39) |
D430G |
probably damaging |
Het |
Prl7d1 |
C |
T |
13: 27,893,240 (GRCm39) |
D224N |
possibly damaging |
Het |
Ptpdc1 |
A |
T |
13: 48,740,173 (GRCm39) |
N419K |
possibly damaging |
Het |
Serinc5 |
T |
A |
13: 92,797,695 (GRCm39) |
|
probably null |
Het |
Sipa1 |
A |
G |
19: 5,701,692 (GRCm39) |
L981P |
probably damaging |
Het |
Slc16a7 |
A |
T |
10: 125,066,489 (GRCm39) |
C383* |
probably null |
Het |
Slc19a1 |
C |
G |
10: 76,878,369 (GRCm39) |
Y301* |
probably null |
Het |
Slc22a14 |
A |
T |
9: 119,052,827 (GRCm39) |
V14E |
possibly damaging |
Het |
Slpi |
C |
A |
2: 164,196,837 (GRCm39) |
C95F |
probably damaging |
Het |
Smurf2 |
G |
A |
11: 106,743,333 (GRCm39) |
H225Y |
possibly damaging |
Het |
Son |
T |
C |
16: 91,452,230 (GRCm39) |
S326P |
possibly damaging |
Het |
Sptb |
T |
A |
12: 76,658,657 (GRCm39) |
K1262M |
probably benign |
Het |
Sugp2 |
T |
A |
8: 70,696,714 (GRCm39) |
|
probably benign |
Het |
Tatdn2 |
T |
A |
6: 113,687,031 (GRCm39) |
H747Q |
probably damaging |
Het |
Tcn2 |
C |
A |
11: 3,877,516 (GRCm39) |
R44L |
probably benign |
Het |
Tenm3 |
G |
A |
8: 48,689,006 (GRCm39) |
R2194C |
probably damaging |
Het |
Tnks2 |
T |
A |
19: 36,822,931 (GRCm39) |
|
probably benign |
Het |
Top3a |
A |
T |
11: 60,650,188 (GRCm39) |
I120N |
probably damaging |
Het |
Umodl1 |
T |
A |
17: 31,201,232 (GRCm39) |
|
probably benign |
Het |
Umodl1 |
T |
C |
17: 31,205,478 (GRCm39) |
V662A |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,595,048 (GRCm39) |
S3827P |
probably benign |
Het |
Vasn |
T |
A |
16: 4,466,473 (GRCm39) |
|
probably null |
Het |
Vmn2r69 |
A |
T |
7: 85,055,908 (GRCm39) |
C743* |
probably null |
Het |
Vmn2r79 |
C |
A |
7: 86,687,002 (GRCm39) |
H794Q |
probably benign |
Het |
|
Other mutations in Itgb4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01360:Itgb4
|
APN |
11 |
115,881,766 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01391:Itgb4
|
APN |
11 |
115,881,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01431:Itgb4
|
APN |
11 |
115,897,283 (GRCm39) |
splice site |
probably benign |
|
IGL01750:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01752:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01756:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01766:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01769:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02188:Itgb4
|
APN |
11 |
115,894,213 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02262:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02293:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02318:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02319:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02338:Itgb4
|
APN |
11 |
115,898,795 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02734:Itgb4
|
APN |
11 |
115,896,792 (GRCm39) |
missense |
probably benign |
|
IGL02879:Itgb4
|
APN |
11 |
115,885,178 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02889:Itgb4
|
APN |
11 |
115,879,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Itgb4
|
APN |
11 |
115,879,550 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03054:Itgb4
|
UTSW |
11 |
115,891,166 (GRCm39) |
nonsense |
probably null |
|
R0021:Itgb4
|
UTSW |
11 |
115,870,453 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0092:Itgb4
|
UTSW |
11 |
115,869,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R0305:Itgb4
|
UTSW |
11 |
115,870,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R0408:Itgb4
|
UTSW |
11 |
115,898,428 (GRCm39) |
missense |
probably damaging |
0.99 |
R0465:Itgb4
|
UTSW |
11 |
115,870,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0499:Itgb4
|
UTSW |
11 |
115,870,521 (GRCm39) |
missense |
probably benign |
0.00 |
R0535:Itgb4
|
UTSW |
11 |
115,881,835 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0571:Itgb4
|
UTSW |
11 |
115,870,594 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0613:Itgb4
|
UTSW |
11 |
115,884,168 (GRCm39) |
missense |
probably damaging |
0.98 |
R0838:Itgb4
|
UTSW |
11 |
115,888,988 (GRCm39) |
intron |
probably benign |
|
R1381:Itgb4
|
UTSW |
11 |
115,885,163 (GRCm39) |
missense |
probably benign |
0.00 |
R1451:Itgb4
|
UTSW |
11 |
115,881,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1460:Itgb4
|
UTSW |
11 |
115,874,990 (GRCm39) |
missense |
probably damaging |
0.96 |
R1473:Itgb4
|
UTSW |
11 |
115,874,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1484:Itgb4
|
UTSW |
11 |
115,890,625 (GRCm39) |
missense |
probably benign |
0.01 |
R1593:Itgb4
|
UTSW |
11 |
115,871,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Itgb4
|
UTSW |
11 |
115,882,142 (GRCm39) |
nonsense |
probably null |
|
R1633:Itgb4
|
UTSW |
11 |
115,898,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R1642:Itgb4
|
UTSW |
11 |
115,898,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R1669:Itgb4
|
UTSW |
11 |
115,882,156 (GRCm39) |
missense |
probably benign |
0.07 |
R1713:Itgb4
|
UTSW |
11 |
115,894,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Itgb4
|
UTSW |
11 |
115,879,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:Itgb4
|
UTSW |
11 |
115,879,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Itgb4
|
UTSW |
11 |
115,874,590 (GRCm39) |
missense |
probably benign |
0.31 |
R1902:Itgb4
|
UTSW |
11 |
115,871,564 (GRCm39) |
missense |
probably damaging |
0.98 |
R1945:Itgb4
|
UTSW |
11 |
115,884,279 (GRCm39) |
nonsense |
probably null |
|
R2102:Itgb4
|
UTSW |
11 |
115,896,561 (GRCm39) |
missense |
probably benign |
0.23 |
R2184:Itgb4
|
UTSW |
11 |
115,870,450 (GRCm39) |
missense |
probably damaging |
0.96 |
R2334:Itgb4
|
UTSW |
11 |
115,884,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R2401:Itgb4
|
UTSW |
11 |
115,897,389 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3743:Itgb4
|
UTSW |
11 |
115,894,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R3938:Itgb4
|
UTSW |
11 |
115,896,752 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4134:Itgb4
|
UTSW |
11 |
115,897,296 (GRCm39) |
missense |
probably benign |
0.03 |
R4280:Itgb4
|
UTSW |
11 |
115,881,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R4342:Itgb4
|
UTSW |
11 |
115,879,555 (GRCm39) |
missense |
probably benign |
0.01 |
R4434:Itgb4
|
UTSW |
11 |
115,890,640 (GRCm39) |
missense |
probably benign |
0.10 |
R4505:Itgb4
|
UTSW |
11 |
115,874,087 (GRCm39) |
splice site |
silent |
|
R4585:Itgb4
|
UTSW |
11 |
115,884,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4586:Itgb4
|
UTSW |
11 |
115,884,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4601:Itgb4
|
UTSW |
11 |
115,896,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Itgb4
|
UTSW |
11 |
115,897,431 (GRCm39) |
missense |
probably benign |
0.12 |
R4962:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5027:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5029:Itgb4
|
UTSW |
11 |
115,879,417 (GRCm39) |
intron |
probably benign |
|
R5084:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5085:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5124:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5125:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5150:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5175:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5176:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5179:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5207:Itgb4
|
UTSW |
11 |
115,897,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R5263:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5264:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5334:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5337:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5344:Itgb4
|
UTSW |
11 |
115,880,575 (GRCm39) |
missense |
probably null |
0.92 |
R5391:Itgb4
|
UTSW |
11 |
115,875,894 (GRCm39) |
missense |
probably benign |
0.05 |
R5437:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5440:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5653:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5654:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5655:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5772:Itgb4
|
UTSW |
11 |
115,879,258 (GRCm39) |
intron |
probably benign |
|
R5812:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5813:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5814:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5863:Itgb4
|
UTSW |
11 |
115,881,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5864:Itgb4
|
UTSW |
11 |
115,881,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5865:Itgb4
|
UTSW |
11 |
115,881,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5951:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5954:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5982:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6043:Itgb4
|
UTSW |
11 |
115,870,212 (GRCm39) |
missense |
probably benign |
0.30 |
R6133:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6134:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6135:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6169:Itgb4
|
UTSW |
11 |
115,885,102 (GRCm39) |
missense |
probably damaging |
0.98 |
R6172:Itgb4
|
UTSW |
11 |
115,891,237 (GRCm39) |
missense |
probably benign |
0.23 |
R6255:Itgb4
|
UTSW |
11 |
115,888,963 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6258:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6259:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6260:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6612:Itgb4
|
UTSW |
11 |
115,874,897 (GRCm39) |
missense |
probably benign |
0.00 |
R7037:Itgb4
|
UTSW |
11 |
115,896,391 (GRCm39) |
nonsense |
probably null |
|
R7371:Itgb4
|
UTSW |
11 |
115,888,906 (GRCm39) |
missense |
probably benign |
0.29 |
R7605:Itgb4
|
UTSW |
11 |
115,897,302 (GRCm39) |
missense |
probably benign |
0.01 |
R7659:Itgb4
|
UTSW |
11 |
115,870,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R7759:Itgb4
|
UTSW |
11 |
115,894,536 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7804:Itgb4
|
UTSW |
11 |
115,894,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R7832:Itgb4
|
UTSW |
11 |
115,891,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Itgb4
|
UTSW |
11 |
115,873,531 (GRCm39) |
missense |
probably benign |
0.18 |
R7923:Itgb4
|
UTSW |
11 |
115,873,525 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8004:Itgb4
|
UTSW |
11 |
115,873,531 (GRCm39) |
missense |
probably benign |
0.00 |
R8143:Itgb4
|
UTSW |
11 |
115,884,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8427:Itgb4
|
UTSW |
11 |
115,882,544 (GRCm39) |
critical splice donor site |
probably null |
|
R8857:Itgb4
|
UTSW |
11 |
115,871,853 (GRCm39) |
missense |
probably benign |
0.04 |
R8863:Itgb4
|
UTSW |
11 |
115,875,898 (GRCm39) |
nonsense |
probably null |
|
R8932:Itgb4
|
UTSW |
11 |
115,879,295 (GRCm39) |
missense |
probably benign |
0.01 |
R9153:Itgb4
|
UTSW |
11 |
115,874,879 (GRCm39) |
missense |
probably benign |
0.00 |
R9207:Itgb4
|
UTSW |
11 |
115,897,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R9239:Itgb4
|
UTSW |
11 |
115,898,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R9267:Itgb4
|
UTSW |
11 |
115,870,465 (GRCm39) |
missense |
probably benign |
|
R9289:Itgb4
|
UTSW |
11 |
115,885,187 (GRCm39) |
missense |
probably benign |
0.01 |
R9328:Itgb4
|
UTSW |
11 |
115,880,625 (GRCm39) |
missense |
probably benign |
0.00 |
R9435:Itgb4
|
UTSW |
11 |
115,895,855 (GRCm39) |
missense |
probably benign |
0.01 |
R9450:Itgb4
|
UTSW |
11 |
115,874,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R9649:Itgb4
|
UTSW |
11 |
115,885,171 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9779:Itgb4
|
UTSW |
11 |
115,882,485 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Itgb4
|
UTSW |
11 |
115,884,278 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Itgb4
|
UTSW |
11 |
115,897,346 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Itgb4
|
UTSW |
11 |
115,888,884 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Itgb4
|
UTSW |
11 |
115,877,637 (GRCm39) |
missense |
probably damaging |
0.99 |
|