Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406C07Rik |
G |
A |
9: 15,196,214 (GRCm39) |
T283M |
probably damaging |
Het |
Abca9 |
A |
G |
11: 110,056,817 (GRCm39) |
M1T |
probably null |
Het |
Ackr1 |
T |
C |
1: 173,159,952 (GRCm39) |
Y189C |
probably damaging |
Het |
Acsm4 |
A |
G |
7: 119,304,264 (GRCm39) |
D303G |
probably benign |
Het |
Arfgef2 |
A |
T |
2: 166,708,867 (GRCm39) |
M1060L |
probably benign |
Het |
Arhgef40 |
T |
A |
14: 52,238,414 (GRCm39) |
F1298I |
probably damaging |
Het |
Atg2a |
T |
C |
19: 6,306,674 (GRCm39) |
I1453T |
probably benign |
Het |
B4galnt1 |
A |
T |
10: 127,007,584 (GRCm39) |
D495V |
probably benign |
Het |
Brpf3 |
T |
A |
17: 29,040,214 (GRCm39) |
D878E |
probably benign |
Het |
C3 |
A |
G |
17: 57,511,015 (GRCm39) |
*1664R |
probably null |
Het |
Cap2 |
A |
G |
13: 46,684,548 (GRCm39) |
T73A |
probably benign |
Het |
Ccr6 |
A |
T |
17: 8,475,394 (GRCm39) |
I200F |
probably damaging |
Het |
Cdc42bpb |
C |
T |
12: 111,274,221 (GRCm39) |
G1021R |
probably benign |
Het |
Cidea |
C |
A |
18: 67,499,485 (GRCm39) |
S124* |
probably null |
Het |
Cnst |
C |
A |
1: 179,420,274 (GRCm39) |
T135K |
probably benign |
Het |
Crebbp |
A |
T |
16: 3,936,952 (GRCm39) |
M805K |
probably benign |
Het |
Crybb1 |
A |
G |
5: 112,411,439 (GRCm39) |
Y119C |
probably damaging |
Het |
Cux1 |
G |
T |
5: 136,402,220 (GRCm39) |
T121K |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 118,049,384 (GRCm39) |
|
probably null |
Het |
Dnmbp |
T |
C |
19: 43,900,677 (GRCm39) |
T48A |
probably damaging |
Het |
Dysf |
G |
A |
6: 84,171,353 (GRCm39) |
G1787E |
probably damaging |
Het |
Gcm2 |
T |
A |
13: 41,258,096 (GRCm39) |
R177S |
probably benign |
Het |
Gdf6 |
G |
T |
4: 9,859,429 (GRCm39) |
R170S |
probably damaging |
Het |
Gm16686 |
A |
T |
4: 88,673,775 (GRCm39) |
M18K |
unknown |
Het |
Gm36864 |
C |
T |
7: 43,886,304 (GRCm39) |
Q179* |
probably null |
Het |
Golgb1 |
A |
G |
16: 36,736,675 (GRCm39) |
D2015G |
probably damaging |
Het |
Gtf2i |
A |
G |
5: 134,324,374 (GRCm39) |
L30P |
probably damaging |
Het |
Herc2 |
A |
G |
7: 55,798,402 (GRCm39) |
E1955G |
possibly damaging |
Het |
Hes3 |
A |
T |
4: 152,372,132 (GRCm39) |
D37E |
probably damaging |
Het |
Igha |
A |
G |
12: 113,223,144 (GRCm39) |
V161A |
probably damaging |
Het |
Isl2 |
T |
G |
9: 55,452,722 (GRCm39) |
S327A |
probably benign |
Het |
Itk |
A |
G |
11: 46,231,539 (GRCm39) |
L339P |
probably damaging |
Het |
Kcnb2 |
T |
C |
1: 15,780,648 (GRCm39) |
S507P |
probably benign |
Het |
Lgals4 |
C |
T |
7: 28,540,921 (GRCm39) |
R282C |
probably damaging |
Het |
Lhfpl4 |
C |
A |
6: 113,171,034 (GRCm39) |
V51L |
possibly damaging |
Het |
Lhpp |
A |
G |
7: 132,243,261 (GRCm39) |
Y159C |
probably damaging |
Het |
Lrwd1 |
C |
A |
5: 136,162,257 (GRCm39) |
E159* |
probably null |
Het |
Map3k13 |
A |
G |
16: 21,745,008 (GRCm39) |
T856A |
probably damaging |
Het |
Mcm8 |
A |
G |
2: 132,665,141 (GRCm39) |
T206A |
probably benign |
Het |
Megf6 |
A |
G |
4: 154,352,436 (GRCm39) |
K1265R |
probably benign |
Het |
Mrgprb2 |
A |
G |
7: 48,202,648 (GRCm39) |
Y26H |
probably benign |
Het |
Mug1 |
T |
C |
6: 121,817,208 (GRCm39) |
|
probably benign |
Het |
Mysm1 |
C |
T |
4: 94,856,196 (GRCm39) |
G134S |
probably damaging |
Het |
Nlrp3 |
A |
C |
11: 59,440,216 (GRCm39) |
I598L |
probably benign |
Het |
Npas2 |
A |
T |
1: 39,331,797 (GRCm39) |
I71F |
possibly damaging |
Het |
Nr1h5 |
A |
G |
3: 102,862,015 (GRCm39) |
S85P |
probably benign |
Het |
Nrcam |
T |
A |
12: 44,619,075 (GRCm39) |
V868D |
possibly damaging |
Het |
Oas1a |
A |
G |
5: 121,040,019 (GRCm39) |
F191L |
probably damaging |
Het |
Or14j8 |
A |
T |
17: 38,263,673 (GRCm39) |
Y81N |
possibly damaging |
Het |
Orc3 |
A |
T |
4: 34,599,778 (GRCm39) |
L125H |
possibly damaging |
Het |
Osbpl7 |
A |
G |
11: 96,946,903 (GRCm39) |
E402G |
possibly damaging |
Het |
Otof |
G |
A |
5: 30,545,968 (GRCm39) |
Q462* |
probably null |
Het |
Phlda2 |
A |
C |
7: 143,055,959 (GRCm39) |
I90S |
probably damaging |
Het |
Plin3 |
C |
T |
17: 56,593,490 (GRCm39) |
V75I |
probably benign |
Het |
Pms1 |
A |
T |
1: 53,321,195 (GRCm39) |
S13T |
possibly damaging |
Het |
Ppm1d |
A |
G |
11: 85,236,732 (GRCm39) |
K504E |
probably damaging |
Het |
Rflna |
A |
T |
5: 125,087,541 (GRCm39) |
I93F |
probably damaging |
Het |
Rnpc3 |
T |
A |
3: 113,414,805 (GRCm39) |
M193L |
probably benign |
Het |
Sema3e |
A |
T |
5: 14,214,169 (GRCm39) |
I145F |
possibly damaging |
Het |
Serpinb1b |
C |
A |
13: 33,271,500 (GRCm39) |
N90K |
probably damaging |
Het |
Sfswap |
A |
G |
5: 129,620,345 (GRCm39) |
D538G |
possibly damaging |
Het |
Snx14 |
A |
T |
9: 88,289,453 (GRCm39) |
D266E |
possibly damaging |
Het |
Stat4 |
C |
T |
1: 52,115,711 (GRCm39) |
T217M |
possibly damaging |
Het |
Taf13 |
T |
C |
3: 108,485,444 (GRCm39) |
M40T |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,523,047 (GRCm39) |
T1530A |
probably damaging |
Het |
Tenm4 |
C |
T |
7: 96,555,148 (GRCm39) |
P2618S |
probably benign |
Het |
Tnfrsf14 |
T |
C |
4: 155,007,710 (GRCm39) |
I220M |
possibly damaging |
Het |
Tnk2 |
T |
C |
16: 32,484,718 (GRCm39) |
W60R |
probably damaging |
Het |
Tph2 |
A |
T |
10: 115,015,614 (GRCm39) |
|
probably benign |
Het |
Upf1 |
C |
G |
8: 70,785,973 (GRCm39) |
M995I |
probably benign |
Het |
Upf1 |
G |
A |
8: 70,785,972 (GRCm39) |
P996S |
probably benign |
Het |
Vcan |
C |
T |
13: 89,840,439 (GRCm39) |
V1702M |
probably benign |
Het |
Vmn2r57 |
T |
C |
7: 41,077,020 (GRCm39) |
D382G |
probably benign |
Het |
Xxylt1 |
C |
T |
16: 30,899,964 (GRCm39) |
A64T |
probably benign |
Het |
Zcchc8 |
A |
G |
5: 123,841,070 (GRCm39) |
S407P |
probably damaging |
Het |
Zdhhc19 |
T |
A |
16: 32,317,187 (GRCm39) |
F109Y |
probably damaging |
Het |
Zfp638 |
T |
C |
6: 83,931,745 (GRCm39) |
|
probably null |
Het |
Zfp691 |
A |
G |
4: 119,027,861 (GRCm39) |
S124P |
probably damaging |
Het |
Zfp804a |
T |
A |
2: 82,089,450 (GRCm39) |
V1093D |
probably damaging |
Het |
Zfp986 |
A |
C |
4: 145,625,550 (GRCm39) |
Q70P |
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 |
|
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 |
|
|