Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arfgap2 |
T |
A |
2: 91,103,906 (GRCm39) |
L334Q |
probably damaging |
Het |
Arhgef18 |
T |
A |
8: 3,436,951 (GRCm39) |
L247Q |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,920,500 (GRCm39) |
C2100S |
probably damaging |
Het |
Bpi |
A |
G |
2: 158,109,670 (GRCm39) |
D206G |
probably benign |
Het |
C6 |
T |
C |
15: 4,761,170 (GRCm39) |
I10T |
possibly damaging |
Het |
Cactin |
A |
G |
10: 81,161,492 (GRCm39) |
T675A |
probably damaging |
Het |
Cd200 |
G |
A |
16: 45,215,157 (GRCm39) |
R165C |
probably benign |
Het |
Cdkal1 |
C |
T |
13: 29,538,777 (GRCm39) |
V461I |
probably benign |
Het |
Ces2g |
C |
T |
8: 105,693,954 (GRCm39) |
S430F |
probably benign |
Het |
Clcn3 |
A |
T |
8: 61,382,522 (GRCm39) |
H382Q |
probably damaging |
Het |
Crem |
A |
T |
18: 3,268,061 (GRCm39) |
V89E |
probably damaging |
Het |
Crtc2 |
T |
A |
3: 90,166,463 (GRCm39) |
M146K |
probably benign |
Het |
Depdc1b |
T |
G |
13: 108,521,316 (GRCm39) |
D374E |
possibly damaging |
Het |
Dgkg |
T |
A |
16: 22,381,519 (GRCm39) |
H477L |
probably benign |
Het |
Dnhd1 |
T |
A |
7: 105,343,174 (GRCm39) |
V1506D |
possibly damaging |
Het |
Erfl |
A |
G |
7: 24,628,682 (GRCm39) |
V60A |
possibly damaging |
Het |
Exosc10 |
G |
A |
4: 148,653,159 (GRCm39) |
|
probably null |
Het |
Fem1al |
T |
C |
11: 29,773,696 (GRCm39) |
E587G |
probably benign |
Het |
Flnb |
G |
T |
14: 7,887,566 (GRCm38) |
G459C |
probably damaging |
Het |
Golgb1 |
A |
G |
16: 36,739,809 (GRCm39) |
D2757G |
probably benign |
Het |
Gsta4 |
T |
G |
9: 78,116,121 (GRCm39) |
|
probably benign |
Het |
Herc2 |
T |
A |
7: 55,700,626 (GRCm39) |
M1K |
probably null |
Het |
Hip1 |
C |
T |
5: 135,450,976 (GRCm39) |
V879M |
probably damaging |
Het |
Htt |
T |
C |
5: 34,983,304 (GRCm39) |
Y968H |
probably benign |
Het |
Ints11 |
T |
A |
4: 155,969,587 (GRCm39) |
Y154* |
probably null |
Het |
Itih5 |
A |
G |
2: 10,195,231 (GRCm39) |
S208G |
probably benign |
Het |
Lamb2 |
C |
T |
9: 108,362,460 (GRCm39) |
T701I |
probably benign |
Het |
Lgals3 |
T |
A |
14: 47,617,557 (GRCm39) |
Y22* |
probably null |
Het |
Macc1 |
T |
A |
12: 119,409,587 (GRCm39) |
D118E |
probably benign |
Het |
Mad2l2 |
T |
C |
4: 148,225,277 (GRCm39) |
L9P |
probably damaging |
Het |
Mark2 |
T |
C |
19: 7,318,571 (GRCm39) |
T6A |
probably benign |
Het |
Mcat |
T |
C |
15: 83,436,812 (GRCm39) |
N143S |
probably benign |
Het |
Med10 |
T |
G |
13: 69,962,046 (GRCm39) |
C144G |
unknown |
Het |
Miga1 |
A |
T |
3: 151,982,460 (GRCm39) |
F539I |
probably damaging |
Het |
Mon2 |
A |
T |
10: 122,849,776 (GRCm39) |
S1174T |
probably benign |
Het |
Mycbp2 |
C |
A |
14: 103,466,871 (GRCm39) |
W1330C |
probably damaging |
Het |
Myo5b |
T |
C |
18: 74,892,169 (GRCm39) |
S1612P |
possibly damaging |
Het |
Nipal4 |
T |
C |
11: 46,052,873 (GRCm39) |
I31V |
probably benign |
Het |
Obox3 |
A |
T |
7: 15,361,226 (GRCm39) |
V13E |
possibly damaging |
Het |
Or2ag19 |
A |
T |
7: 106,444,636 (GRCm39) |
I273F |
probably damaging |
Het |
Or8g4 |
T |
C |
9: 39,661,994 (GRCm39) |
F104S |
probably damaging |
Het |
Ppic |
A |
G |
18: 53,542,222 (GRCm39) |
V162A |
probably damaging |
Het |
Prkg2 |
T |
C |
5: 99,090,043 (GRCm39) |
K699R |
probably benign |
Het |
Prl2c2 |
T |
A |
13: 13,179,656 (GRCm39) |
L6F |
possibly damaging |
Het |
Rnf148 |
G |
C |
6: 23,654,378 (GRCm39) |
S206C |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,313,586 (GRCm39) |
S474P |
|
Het |
Sema5a |
T |
G |
15: 32,689,498 (GRCm39) |
H1054Q |
probably benign |
Het |
Slc6a18 |
C |
A |
13: 73,813,751 (GRCm39) |
V521F |
probably null |
Het |
Stat2 |
T |
A |
10: 128,127,233 (GRCm39) |
D921E |
possibly damaging |
Het |
Tcf24 |
G |
T |
1: 10,031,224 (GRCm39) |
N42K |
unknown |
Het |
Tgfb2 |
T |
A |
1: 186,361,136 (GRCm39) |
N372Y |
probably damaging |
Het |
Tktl2 |
A |
C |
8: 66,966,319 (GRCm39) |
M626L |
possibly damaging |
Het |
Tmem94 |
A |
G |
11: 115,688,201 (GRCm39) |
D1220G |
probably benign |
Het |
Trcg1 |
A |
G |
9: 57,148,754 (GRCm39) |
T109A |
probably benign |
Het |
Trim30a |
T |
A |
7: 104,060,529 (GRCm39) |
K416* |
probably null |
Het |
Trpm5 |
T |
C |
7: 142,636,753 (GRCm39) |
K395E |
possibly damaging |
Het |
Ufm1 |
T |
A |
3: 53,771,093 (GRCm39) |
|
probably null |
Het |
Vmn2r16 |
T |
C |
5: 109,487,019 (GRCm39) |
V80A |
probably benign |
Het |
Vmn2r77 |
A |
T |
7: 86,452,855 (GRCm39) |
Y524F |
probably benign |
Het |
Zfp1007 |
T |
G |
5: 109,826,746 (GRCm39) |
T5P |
probably damaging |
Het |
Zfp64 |
T |
C |
2: 168,793,552 (GRCm39) |
S65G |
probably benign |
Het |
Zng1 |
A |
G |
19: 24,926,601 (GRCm39) |
V150A |
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 |
|
R7424:Unc13b
|
UTSW |
4 |
43,172,235 (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 |
|
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 |
|
|