Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
C |
T |
8: 120,872,284 (GRCm39) |
R71C |
probably damaging |
Het |
Aanat |
A |
T |
11: 116,486,455 (GRCm39) |
|
probably benign |
Het |
Ahrr |
G |
T |
13: 74,405,664 (GRCm39) |
S91* |
probably null |
Het |
Ampd1 |
A |
T |
3: 102,995,758 (GRCm39) |
N223Y |
probably benign |
Het |
Ankar |
T |
G |
1: 72,719,217 (GRCm39) |
N544T |
probably damaging |
Het |
Ankk1 |
A |
G |
9: 49,330,050 (GRCm39) |
S302P |
possibly damaging |
Het |
Bcr |
T |
C |
10: 74,992,932 (GRCm39) |
V809A |
probably benign |
Het |
Bpifb2 |
A |
G |
2: 153,732,460 (GRCm39) |
N353S |
possibly damaging |
Het |
Cyth1 |
A |
T |
11: 118,074,835 (GRCm39) |
|
probably null |
Het |
Ddx5 |
A |
T |
11: 106,673,006 (GRCm39) |
N506K |
probably benign |
Het |
Dnaja1 |
A |
T |
4: 40,730,244 (GRCm39) |
I239F |
probably benign |
Het |
Ethe1 |
C |
T |
7: 24,305,676 (GRCm39) |
T141I |
probably damaging |
Het |
Fhip2b |
T |
C |
14: 70,831,447 (GRCm39) |
H29R |
probably damaging |
Het |
Gdap2 |
A |
T |
3: 100,109,382 (GRCm39) |
I36F |
unknown |
Het |
Gm13030 |
A |
T |
4: 138,598,577 (GRCm39) |
D115E |
unknown |
Het |
Gm17019 |
A |
T |
5: 15,079,386 (GRCm39) |
L227Q |
probably damaging |
Het |
Gm9195 |
T |
A |
14: 72,673,217 (GRCm39) |
E2517D |
possibly damaging |
Het |
Gramd2a |
T |
A |
9: 59,615,354 (GRCm39) |
V39D |
possibly damaging |
Het |
Hmcn1 |
C |
T |
1: 150,506,017 (GRCm39) |
W3836* |
probably null |
Het |
Hspa14 |
C |
T |
2: 3,490,078 (GRCm39) |
D494N |
possibly damaging |
Het |
Ifit2 |
A |
G |
19: 34,550,598 (GRCm39) |
N46S |
probably benign |
Het |
Ifna6 |
A |
T |
4: 88,746,044 (GRCm39) |
E131V |
possibly damaging |
Het |
Ift140 |
T |
C |
17: 25,256,010 (GRCm39) |
V504A |
possibly damaging |
Het |
Irgc |
T |
C |
7: 24,131,653 (GRCm39) |
N388S |
probably damaging |
Het |
Itgal |
T |
A |
7: 126,916,537 (GRCm39) |
V743E |
probably benign |
Het |
Itih5 |
T |
C |
2: 10,250,448 (GRCm39) |
S716P |
probably damaging |
Het |
Kcnab1 |
A |
T |
3: 65,173,924 (GRCm39) |
K78N |
possibly damaging |
Het |
Kif1a |
A |
T |
1: 92,982,039 (GRCm39) |
V787E |
possibly damaging |
Het |
Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
Krt39 |
A |
T |
11: 99,408,917 (GRCm39) |
V293E |
probably damaging |
Het |
Lrrn4 |
A |
G |
2: 132,711,663 (GRCm39) |
F720S |
possibly damaging |
Het |
Map2 |
G |
A |
1: 66,453,983 (GRCm39) |
A958T |
possibly damaging |
Het |
Map3k9 |
A |
G |
12: 81,770,871 (GRCm39) |
S906P |
probably benign |
Het |
Mdc1 |
T |
C |
17: 36,164,201 (GRCm39) |
S1250P |
probably benign |
Het |
Meltf |
G |
A |
16: 31,703,764 (GRCm39) |
V164I |
probably damaging |
Het |
Mtap |
T |
G |
4: 89,097,699 (GRCm39) |
|
probably null |
Het |
Mtus1 |
C |
A |
8: 41,475,443 (GRCm39) |
V184F |
probably damaging |
Het |
Myh1 |
A |
T |
11: 67,104,489 (GRCm39) |
D1015V |
probably damaging |
Het |
Ndrg1 |
T |
C |
15: 66,816,787 (GRCm39) |
|
probably null |
Het |
Nkd1 |
G |
T |
8: 89,311,803 (GRCm39) |
V130L |
probably benign |
Het |
Nsfl1c |
A |
G |
2: 151,342,673 (GRCm39) |
D81G |
probably benign |
Het |
Nt5c1b |
T |
A |
12: 10,431,391 (GRCm39) |
|
probably null |
Het |
Nucb1 |
T |
C |
7: 45,148,202 (GRCm39) |
K204E |
possibly damaging |
Het |
Nwd1 |
T |
G |
8: 73,401,801 (GRCm39) |
M774R |
possibly damaging |
Het |
Or2m13 |
A |
T |
16: 19,225,944 (GRCm39) |
V274E |
probably damaging |
Het |
Or52u1 |
G |
C |
7: 104,237,907 (GRCm39) |
E299Q |
probably damaging |
Het |
Or5an1c |
A |
T |
19: 12,218,318 (GRCm39) |
S236T |
possibly damaging |
Het |
Pan3 |
T |
A |
5: 147,473,082 (GRCm39) |
|
probably null |
Het |
Pcdh15 |
A |
T |
10: 74,342,317 (GRCm39) |
T1135S |
probably benign |
Het |
Pfas |
A |
G |
11: 68,890,918 (GRCm39) |
I331T |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,488,647 (GRCm39) |
I1641N |
probably damaging |
Het |
Pramel27 |
C |
T |
4: 143,579,779 (GRCm39) |
P455S |
probably benign |
Het |
Ptar1 |
A |
T |
19: 23,695,465 (GRCm39) |
R311W |
probably damaging |
Het |
Ranbp2 |
T |
G |
10: 58,315,016 (GRCm39) |
M1912R |
probably damaging |
Het |
Rbm12 |
A |
G |
2: 155,939,223 (GRCm39) |
F350L |
possibly damaging |
Het |
Sdhaf1 |
T |
C |
7: 30,021,468 (GRCm39) |
D96G |
probably benign |
Het |
Serpinb6b |
T |
A |
13: 33,152,650 (GRCm39) |
M53K |
probably damaging |
Het |
Sh2d6 |
A |
T |
6: 72,494,147 (GRCm39) |
L147Q |
probably benign |
Het |
Slc19a2 |
T |
A |
1: 164,088,445 (GRCm39) |
C298S |
probably benign |
Het |
Son |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,222 (GRCm39) |
|
probably benign |
Het |
St8sia2 |
T |
A |
7: 73,610,650 (GRCm39) |
Q211L |
possibly damaging |
Het |
Sult2a2 |
T |
C |
7: 13,468,822 (GRCm39) |
I96T |
possibly damaging |
Het |
Tab2 |
G |
T |
10: 7,783,247 (GRCm39) |
H678Q |
probably damaging |
Het |
Tnfaip6 |
A |
G |
2: 51,928,228 (GRCm39) |
E14G |
probably benign |
Het |
Trip11 |
A |
T |
12: 101,851,457 (GRCm39) |
L869H |
probably damaging |
Het |
Tslp |
T |
C |
18: 32,952,133 (GRCm39) |
Y133H |
not run |
Het |
Ttn |
T |
C |
2: 76,571,334 (GRCm39) |
I26520V |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,762,487 (GRCm39) |
V3374A |
unknown |
Het |
Tubgcp2 |
T |
A |
7: 139,587,837 (GRCm39) |
I263F |
possibly damaging |
Het |
Uaca |
A |
G |
9: 60,777,392 (GRCm39) |
E593G |
probably damaging |
Het |
Ush1c |
T |
A |
7: 45,874,979 (GRCm39) |
I131F |
probably benign |
Het |
Usp24 |
C |
A |
4: 106,236,304 (GRCm39) |
D997E |
probably benign |
Het |
Usp54 |
T |
C |
14: 20,627,108 (GRCm39) |
T517A |
probably benign |
Het |
Vmn1r151 |
A |
T |
7: 22,198,505 (GRCm39) |
M200K |
possibly damaging |
Het |
Vmn2r43 |
T |
C |
7: 8,258,328 (GRCm39) |
D295G |
probably damaging |
Het |
Vmn2r70 |
G |
A |
7: 85,213,076 (GRCm39) |
P444S |
probably damaging |
Het |
Vmn2r85 |
G |
T |
10: 130,254,849 (GRCm39) |
P612T |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,875,317 (GRCm39) |
V1736D |
|
Het |
Zbtb11 |
A |
T |
16: 55,810,850 (GRCm39) |
H336L |
probably benign |
Het |
|
Other mutations in Unc13b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Unc13b
|
APN |
4 |
43,240,285 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00832:Unc13b
|
APN |
4 |
43,258,921 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01111:Unc13b
|
APN |
4 |
43,096,927 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01115:Unc13b
|
APN |
4 |
43,258,492 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01137:Unc13b
|
APN |
4 |
43,091,291 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01637:Unc13b
|
APN |
4 |
43,241,066 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01789:Unc13b
|
APN |
4 |
43,239,462 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01792:Unc13b
|
APN |
4 |
43,250,218 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01877:Unc13b
|
APN |
4 |
43,249,583 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01924:Unc13b
|
APN |
4 |
43,239,385 (GRCm39) |
nonsense |
probably null |
|
IGL02087:Unc13b
|
APN |
4 |
43,091,270 (GRCm39) |
missense |
probably null |
1.00 |
IGL02197:Unc13b
|
APN |
4 |
43,165,828 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02504:Unc13b
|
APN |
4 |
43,263,031 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02659:Unc13b
|
APN |
4 |
43,235,332 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03031:Unc13b
|
APN |
4 |
43,235,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03036:Unc13b
|
APN |
4 |
43,235,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03209:Unc13b
|
APN |
4 |
43,239,351 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03352:Unc13b
|
APN |
4 |
43,237,110 (GRCm39) |
missense |
possibly damaging |
0.90 |
BB006:Unc13b
|
UTSW |
4 |
43,174,399 (GRCm39) |
missense |
unknown |
|
BB016:Unc13b
|
UTSW |
4 |
43,174,399 (GRCm39) |
missense |
unknown |
|
G1Funyon:Unc13b
|
UTSW |
4 |
43,263,568 (GRCm39) |
missense |
probably benign |
|
P0028:Unc13b
|
UTSW |
4 |
43,256,225 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4585001:Unc13b
|
UTSW |
4 |
43,091,298 (GRCm39) |
missense |
probably benign |
0.03 |
R0019:Unc13b
|
UTSW |
4 |
43,096,990 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0019:Unc13b
|
UTSW |
4 |
43,096,990 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0335:Unc13b
|
UTSW |
4 |
43,236,983 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0504:Unc13b
|
UTSW |
4 |
43,263,559 (GRCm39) |
missense |
probably damaging |
0.99 |
R0631:Unc13b
|
UTSW |
4 |
43,182,849 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0748:Unc13b
|
UTSW |
4 |
43,241,164 (GRCm39) |
splice site |
probably benign |
|
R1275:Unc13b
|
UTSW |
4 |
43,235,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R1293:Unc13b
|
UTSW |
4 |
43,235,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Unc13b
|
UTSW |
4 |
43,239,385 (GRCm39) |
nonsense |
probably null |
|
R1552:Unc13b
|
UTSW |
4 |
43,237,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R1591:Unc13b
|
UTSW |
4 |
43,244,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R1628:Unc13b
|
UTSW |
4 |
43,263,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R1740:Unc13b
|
UTSW |
4 |
43,240,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R1839:Unc13b
|
UTSW |
4 |
43,258,308 (GRCm39) |
splice site |
probably benign |
|
R2045:Unc13b
|
UTSW |
4 |
43,091,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Unc13b
|
UTSW |
4 |
43,245,566 (GRCm39) |
nonsense |
probably null |
|
R2259:Unc13b
|
UTSW |
4 |
43,182,780 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2307:Unc13b
|
UTSW |
4 |
43,239,854 (GRCm39) |
missense |
probably damaging |
0.98 |
R2317:Unc13b
|
UTSW |
4 |
43,245,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R2402:Unc13b
|
UTSW |
4 |
43,095,843 (GRCm39) |
missense |
probably benign |
|
R2847:Unc13b
|
UTSW |
4 |
43,180,404 (GRCm39) |
missense |
probably benign |
0.04 |
R3414:Unc13b
|
UTSW |
4 |
43,234,658 (GRCm39) |
splice site |
probably benign |
|
R3436:Unc13b
|
UTSW |
4 |
43,097,028 (GRCm39) |
splice site |
probably benign |
|
R3955:Unc13b
|
UTSW |
4 |
43,256,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R3957:Unc13b
|
UTSW |
4 |
43,256,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R4015:Unc13b
|
UTSW |
4 |
43,237,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R4650:Unc13b
|
UTSW |
4 |
43,261,035 (GRCm39) |
missense |
probably damaging |
0.97 |
R4836:Unc13b
|
UTSW |
4 |
43,237,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R5041:Unc13b
|
UTSW |
4 |
43,237,836 (GRCm39) |
missense |
probably benign |
0.41 |
R5413:Unc13b
|
UTSW |
4 |
43,257,936 (GRCm39) |
critical splice donor site |
probably null |
|
R5994:Unc13b
|
UTSW |
4 |
43,172,596 (GRCm39) |
intron |
probably benign |
|
R6015:Unc13b
|
UTSW |
4 |
43,177,995 (GRCm39) |
nonsense |
probably null |
|
R6090:Unc13b
|
UTSW |
4 |
43,239,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Unc13b
|
UTSW |
4 |
43,165,800 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6246:Unc13b
|
UTSW |
4 |
43,216,246 (GRCm39) |
missense |
probably benign |
0.18 |
R6427:Unc13b
|
UTSW |
4 |
43,176,966 (GRCm39) |
unclassified |
probably benign |
|
R6660:Unc13b
|
UTSW |
4 |
43,177,412 (GRCm39) |
unclassified |
probably benign |
|
R6670:Unc13b
|
UTSW |
4 |
43,255,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R6753:Unc13b
|
UTSW |
4 |
43,239,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R6858:Unc13b
|
UTSW |
4 |
43,165,828 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6886:Unc13b
|
UTSW |
4 |
43,170,156 (GRCm39) |
intron |
probably benign |
|
R6969:Unc13b
|
UTSW |
4 |
43,263,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6994:Unc13b
|
UTSW |
4 |
43,173,203 (GRCm39) |
intron |
probably benign |
|
R6994:Unc13b
|
UTSW |
4 |
43,171,403 (GRCm39) |
intron |
probably benign |
|
R7080:Unc13b
|
UTSW |
4 |
43,171,926 (GRCm39) |
missense |
unknown |
|
R7117:Unc13b
|
UTSW |
4 |
43,216,544 (GRCm39) |
missense |
probably benign |
0.33 |
R7132:Unc13b
|
UTSW |
4 |
43,215,757 (GRCm39) |
missense |
probably benign |
0.17 |
R7181:Unc13b
|
UTSW |
4 |
43,258,893 (GRCm39) |
missense |
probably damaging |
0.99 |
R7192:Unc13b
|
UTSW |
4 |
43,258,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R7246:Unc13b
|
UTSW |
4 |
43,172,910 (GRCm39) |
missense |
unknown |
|
R7342:Unc13b
|
UTSW |
4 |
43,258,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R7345:Unc13b
|
UTSW |
4 |
43,173,966 (GRCm39) |
missense |
unknown |
|
R7355:Unc13b
|
UTSW |
4 |
43,237,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Unc13b
|
UTSW |
4 |
43,216,459 (GRCm39) |
missense |
probably benign |
0.03 |
R7419:Unc13b
|
UTSW |
4 |
43,174,023 (GRCm39) |
missense |
unknown |
|
R7517:Unc13b
|
UTSW |
4 |
43,215,765 (GRCm39) |
missense |
probably benign |
|
R7532:Unc13b
|
UTSW |
4 |
43,249,565 (GRCm39) |
missense |
probably benign |
0.44 |
R7564:Unc13b
|
UTSW |
4 |
43,091,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7598:Unc13b
|
UTSW |
4 |
43,263,569 (GRCm39) |
missense |
probably benign |
0.20 |
R7604:Unc13b
|
UTSW |
4 |
43,256,776 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7604:Unc13b
|
UTSW |
4 |
43,170,102 (GRCm39) |
missense |
unknown |
|
R7643:Unc13b
|
UTSW |
4 |
43,216,333 (GRCm39) |
missense |
probably benign |
|
R7718:Unc13b
|
UTSW |
4 |
43,173,854 (GRCm39) |
missense |
unknown |
|
R7735:Unc13b
|
UTSW |
4 |
43,165,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R7756:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small deletion |
probably benign |
|
R7757:Unc13b
|
UTSW |
4 |
43,177,341 (GRCm39) |
small insertion |
probably benign |
|
R7757:Unc13b
|
UTSW |
4 |
43,177,330 (GRCm39) |
small insertion |
probably benign |
|
R7757:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small deletion |
probably benign |
|
R7758:Unc13b
|
UTSW |
4 |
43,177,344 (GRCm39) |
small insertion |
probably benign |
|
R7758:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small insertion |
probably benign |
|
R7781:Unc13b
|
UTSW |
4 |
43,259,546 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7793:Unc13b
|
UTSW |
4 |
43,172,737 (GRCm39) |
missense |
unknown |
|
R7858:Unc13b
|
UTSW |
4 |
43,176,285 (GRCm39) |
missense |
unknown |
|
R7867:Unc13b
|
UTSW |
4 |
43,232,573 (GRCm39) |
nonsense |
probably null |
|
R7897:Unc13b
|
UTSW |
4 |
43,171,860 (GRCm39) |
missense |
unknown |
|
R7904:Unc13b
|
UTSW |
4 |
43,217,075 (GRCm39) |
missense |
probably benign |
|
R7929:Unc13b
|
UTSW |
4 |
43,174,399 (GRCm39) |
missense |
unknown |
|
R7984:Unc13b
|
UTSW |
4 |
43,173,973 (GRCm39) |
missense |
unknown |
|
R8069:Unc13b
|
UTSW |
4 |
43,177,597 (GRCm39) |
missense |
unknown |
|
R8101:Unc13b
|
UTSW |
4 |
43,239,918 (GRCm39) |
missense |
probably benign |
0.08 |
R8246:Unc13b
|
UTSW |
4 |
43,175,954 (GRCm39) |
missense |
unknown |
|
R8289:Unc13b
|
UTSW |
4 |
43,172,524 (GRCm39) |
nonsense |
probably null |
|
R8301:Unc13b
|
UTSW |
4 |
43,263,568 (GRCm39) |
missense |
probably benign |
|
R8397:Unc13b
|
UTSW |
4 |
43,217,290 (GRCm39) |
missense |
probably benign |
0.12 |
R8421:Unc13b
|
UTSW |
4 |
43,178,304 (GRCm39) |
missense |
unknown |
|
R8738:Unc13b
|
UTSW |
4 |
43,177,564 (GRCm39) |
missense |
unknown |
|
R8746:Unc13b
|
UTSW |
4 |
43,176,120 (GRCm39) |
missense |
unknown |
|
R8766:Unc13b
|
UTSW |
4 |
43,174,722 (GRCm39) |
missense |
unknown |
|
R8825:Unc13b
|
UTSW |
4 |
43,237,683 (GRCm39) |
splice site |
probably benign |
|
R8834:Unc13b
|
UTSW |
4 |
43,175,954 (GRCm39) |
missense |
unknown |
|
R8862:Unc13b
|
UTSW |
4 |
43,235,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Unc13b
|
UTSW |
4 |
43,174,724 (GRCm39) |
missense |
unknown |
|
R8889:Unc13b
|
UTSW |
4 |
43,176,484 (GRCm39) |
missense |
unknown |
|
R8892:Unc13b
|
UTSW |
4 |
43,176,484 (GRCm39) |
missense |
unknown |
|
R8904:Unc13b
|
UTSW |
4 |
43,178,531 (GRCm39) |
intron |
probably benign |
|
R9089:Unc13b
|
UTSW |
4 |
43,095,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R9144:Unc13b
|
UTSW |
4 |
43,173,649 (GRCm39) |
missense |
unknown |
|
R9149:Unc13b
|
UTSW |
4 |
43,176,186 (GRCm39) |
missense |
unknown |
|
R9173:Unc13b
|
UTSW |
4 |
43,177,421 (GRCm39) |
missense |
unknown |
|
R9200:Unc13b
|
UTSW |
4 |
43,257,352 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9232:Unc13b
|
UTSW |
4 |
43,240,321 (GRCm39) |
missense |
probably benign |
0.03 |
R9269:Unc13b
|
UTSW |
4 |
43,171,955 (GRCm39) |
missense |
unknown |
|
R9320:Unc13b
|
UTSW |
4 |
43,171,044 (GRCm39) |
missense |
unknown |
|
R9335:Unc13b
|
UTSW |
4 |
43,255,551 (GRCm39) |
missense |
probably damaging |
0.99 |
R9335:Unc13b
|
UTSW |
4 |
43,216,123 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9352:Unc13b
|
UTSW |
4 |
43,177,313 (GRCm39) |
nonsense |
probably null |
|
R9352:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small insertion |
probably benign |
|
R9378:Unc13b
|
UTSW |
4 |
43,173,282 (GRCm39) |
missense |
unknown |
|
R9382:Unc13b
|
UTSW |
4 |
43,172,512 (GRCm39) |
missense |
unknown |
|
R9569:Unc13b
|
UTSW |
4 |
43,177,312 (GRCm39) |
small deletion |
probably benign |
|
R9622:Unc13b
|
UTSW |
4 |
43,172,513 (GRCm39) |
missense |
|
|
R9687:Unc13b
|
UTSW |
4 |
43,174,920 (GRCm39) |
missense |
unknown |
|
R9704:Unc13b
|
UTSW |
4 |
43,237,102 (GRCm39) |
missense |
probably benign |
0.31 |
R9721:Unc13b
|
UTSW |
4 |
43,101,869 (GRCm39) |
missense |
probably benign |
|
R9753:Unc13b
|
UTSW |
4 |
43,182,842 (GRCm39) |
nonsense |
probably null |
|
RF016:Unc13b
|
UTSW |
4 |
43,177,350 (GRCm39) |
small insertion |
probably benign |
|
RF016:Unc13b
|
UTSW |
4 |
43,177,347 (GRCm39) |
small insertion |
probably benign |
|
RF041:Unc13b
|
UTSW |
4 |
43,177,338 (GRCm39) |
small insertion |
probably benign |
|
RF056:Unc13b
|
UTSW |
4 |
43,177,359 (GRCm39) |
small insertion |
probably benign |
|
Z1176:Unc13b
|
UTSW |
4 |
43,177,764 (GRCm39) |
missense |
unknown |
|
Z1176:Unc13b
|
UTSW |
4 |
43,177,191 (GRCm39) |
missense |
unknown |
|
Z1176:Unc13b
|
UTSW |
4 |
43,171,419 (GRCm39) |
missense |
unknown |
|
Z1176:Unc13b
|
UTSW |
4 |
43,261,043 (GRCm39) |
missense |
probably benign |
0.11 |
Z1177:Unc13b
|
UTSW |
4 |
43,173,669 (GRCm39) |
missense |
unknown |
|
|