Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410137M14Rik |
T |
A |
17: 37,289,412 (GRCm39) |
I105F |
possibly damaging |
Het |
Adprhl1 |
C |
T |
8: 13,298,682 (GRCm39) |
V83I |
probably damaging |
Het |
Adra1d |
G |
T |
2: 131,403,600 (GRCm39) |
C163* |
probably null |
Het |
Ak9 |
A |
G |
10: 41,259,944 (GRCm39) |
D874G |
|
Het |
Akap8 |
A |
T |
17: 32,528,419 (GRCm39) |
S498T |
probably damaging |
Het |
Alyref2 |
C |
G |
1: 171,331,407 (GRCm39) |
F61L |
probably benign |
Het |
Ank1 |
A |
T |
8: 23,606,123 (GRCm39) |
I1172F |
probably damaging |
Het |
Ankrd50 |
A |
T |
3: 38,511,258 (GRCm39) |
F370I |
probably damaging |
Het |
Apip |
A |
C |
2: 102,913,366 (GRCm39) |
T41P |
probably benign |
Het |
Atg4d |
G |
A |
9: 21,178,260 (GRCm39) |
R126Q |
probably null |
Het |
Ccdc86 |
A |
G |
19: 10,926,183 (GRCm39) |
S139P |
unknown |
Het |
Ceacam16 |
A |
G |
7: 19,587,556 (GRCm39) |
L404P |
probably damaging |
Het |
Dennd3 |
G |
T |
15: 73,436,423 (GRCm39) |
V1010L |
probably damaging |
Het |
Disp1 |
A |
G |
1: 182,917,103 (GRCm39) |
S108P |
probably benign |
Het |
Ecpas |
A |
G |
4: 58,869,554 (GRCm39) |
C238R |
probably damaging |
Het |
Ephb2 |
A |
G |
4: 136,388,195 (GRCm39) |
V635A |
probably damaging |
Het |
G530012D18Rik |
C |
G |
1: 85,504,935 (GRCm39) |
D113E |
unknown |
Het |
Gars1 |
A |
G |
6: 55,040,102 (GRCm39) |
H343R |
probably damaging |
Het |
Gli2 |
A |
T |
1: 118,769,772 (GRCm39) |
N593K |
possibly damaging |
Het |
Il18rap |
T |
A |
1: 40,570,740 (GRCm39) |
N227K |
probably damaging |
Het |
Il4ra |
T |
C |
7: 125,174,348 (GRCm39) |
S297P |
probably benign |
Het |
Itprid1 |
G |
A |
6: 55,874,946 (GRCm39) |
V299M |
probably damaging |
Het |
Jak1 |
A |
T |
4: 101,011,842 (GRCm39) |
F1087I |
probably damaging |
Het |
Klf16 |
A |
G |
10: 80,412,698 (GRCm39) |
S113P |
probably benign |
Het |
Klhl30 |
A |
T |
1: 91,283,238 (GRCm39) |
E280V |
possibly damaging |
Het |
Kti12 |
A |
C |
4: 108,705,443 (GRCm39) |
E119A |
probably benign |
Het |
Kti12 |
G |
T |
4: 108,705,444 (GRCm39) |
E119D |
probably benign |
Het |
Lama4 |
A |
G |
10: 38,954,843 (GRCm39) |
H1132R |
probably damaging |
Het |
Lmtk3 |
A |
G |
7: 45,444,572 (GRCm39) |
D1085G |
unknown |
Het |
Lrrc9 |
C |
A |
12: 72,533,071 (GRCm39) |
T980K |
possibly damaging |
Het |
Nceh1 |
A |
G |
3: 27,333,396 (GRCm39) |
D164G |
probably benign |
Het |
Nlrp2 |
A |
G |
7: 5,330,498 (GRCm39) |
S633P |
probably damaging |
Het |
Nxn |
A |
G |
11: 76,164,863 (GRCm39) |
V216A |
possibly damaging |
Het |
Odf4 |
A |
T |
11: 68,813,759 (GRCm39) |
V143D |
possibly damaging |
Het |
Or4d6 |
G |
A |
19: 12,086,118 (GRCm39) |
T38I |
unknown |
Het |
Pex12 |
A |
G |
11: 83,188,809 (GRCm39) |
I62T |
probably damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Plekhg1 |
G |
A |
10: 3,869,170 (GRCm39) |
D237N |
probably damaging |
Het |
Rxrb |
T |
A |
17: 34,255,645 (GRCm39) |
D377E |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,609,680 (GRCm39) |
D4382V |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,705,181 (GRCm39) |
K2862* |
probably null |
Het |
Ryr3 |
A |
G |
2: 112,664,533 (GRCm39) |
L1606P |
probably benign |
Het |
Samd3 |
A |
G |
10: 26,127,813 (GRCm39) |
K270R |
probably damaging |
Het |
Slc2a5 |
C |
A |
4: 150,223,942 (GRCm39) |
F211L |
probably benign |
Het |
Spata31 |
T |
A |
13: 65,069,532 (GRCm39) |
V560D |
probably benign |
Het |
Tbk1 |
A |
G |
10: 121,393,138 (GRCm39) |
C471R |
probably benign |
Het |
Tbx20 |
A |
T |
9: 24,637,059 (GRCm39) |
S343T |
possibly damaging |
Het |
Tesk2 |
A |
G |
4: 116,659,452 (GRCm39) |
E304G |
probably benign |
Het |
Tle1 |
A |
G |
4: 72,118,239 (GRCm39) |
F2L |
possibly damaging |
Het |
Tle4 |
G |
T |
19: 14,495,244 (GRCm39) |
P162T |
probably benign |
Het |
Ttn |
G |
A |
2: 76,673,816 (GRCm39) |
P11172S |
unknown |
Het |
Tulp1 |
T |
C |
17: 28,572,746 (GRCm39) |
N470S |
possibly damaging |
Het |
Vmn2r107 |
T |
G |
17: 20,565,706 (GRCm39) |
I7S |
probably null |
Het |
Vmn2r91 |
T |
G |
17: 18,327,906 (GRCm39) |
I500R |
probably damaging |
Het |
Xpnpep3 |
A |
G |
15: 81,311,626 (GRCm39) |
I111V |
probably damaging |
Het |
Zp3r |
T |
A |
1: 130,519,217 (GRCm39) |
E308V |
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 |
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 |
|
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 |
|
|