Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
A |
G |
13: 81,707,543 (GRCm39) |
F568L |
probably benign |
Het |
AW112010 |
T |
A |
19: 11,025,741 (GRCm39) |
|
noncoding transcript |
Het |
Bbs4 |
A |
T |
9: 59,237,729 (GRCm39) |
L205H |
probably benign |
Het |
Bmal2 |
T |
C |
6: 146,711,266 (GRCm39) |
V90A |
possibly damaging |
Het |
C2cd2l |
T |
C |
9: 44,227,878 (GRCm39) |
K121R |
probably benign |
Het |
Car14 |
A |
G |
3: 95,806,870 (GRCm39) |
V198A |
possibly damaging |
Het |
Cd22 |
G |
T |
7: 30,576,955 (GRCm39) |
H117Q |
possibly damaging |
Het |
Celf1 |
T |
A |
2: 90,829,068 (GRCm39) |
I45N |
probably damaging |
Het |
Cluh |
T |
C |
11: 74,547,997 (GRCm39) |
S103P |
probably damaging |
Het |
Cyp39a1 |
T |
A |
17: 44,002,613 (GRCm39) |
L276Q |
probably benign |
Het |
Ddx27 |
T |
G |
2: 166,857,245 (GRCm39) |
|
probably benign |
Het |
Defb4 |
A |
T |
8: 19,251,279 (GRCm39) |
I49F |
possibly damaging |
Het |
Dock8 |
C |
A |
19: 25,055,509 (GRCm39) |
T157K |
probably benign |
Het |
Dpp6 |
T |
C |
5: 27,839,541 (GRCm39) |
V352A |
probably damaging |
Het |
Elmo2 |
C |
T |
2: 165,139,312 (GRCm39) |
E412K |
probably damaging |
Het |
Eme1 |
G |
A |
11: 94,541,733 (GRCm39) |
P30S |
possibly damaging |
Het |
Espnl |
G |
T |
1: 91,272,535 (GRCm39) |
A632S |
probably benign |
Het |
Gfod1 |
C |
A |
13: 43,354,211 (GRCm39) |
A255S |
probably benign |
Het |
Helz2 |
T |
A |
2: 180,872,704 (GRCm39) |
K2432M |
probably damaging |
Het |
Idua |
T |
C |
5: 108,827,657 (GRCm39) |
L157P |
probably damaging |
Het |
Ifi207 |
T |
A |
1: 173,555,159 (GRCm39) |
D848V |
probably damaging |
Het |
Jag1 |
C |
T |
2: 136,927,858 (GRCm39) |
S851N |
possibly damaging |
Het |
Kat6b |
T |
A |
14: 21,681,415 (GRCm39) |
F571I |
probably damaging |
Het |
Lrrc74b |
G |
A |
16: 17,376,028 (GRCm39) |
|
probably benign |
Het |
Mst1r |
A |
G |
9: 107,794,026 (GRCm39) |
K1160E |
probably damaging |
Het |
Muc19 |
C |
A |
15: 91,778,192 (GRCm39) |
|
noncoding transcript |
Het |
Nrg4 |
G |
A |
9: 55,135,198 (GRCm39) |
|
probably benign |
Het |
Ociad1 |
T |
C |
5: 73,458,037 (GRCm39) |
I12T |
possibly damaging |
Het |
Or1o3 |
A |
G |
17: 37,574,111 (GRCm39) |
V148A |
possibly damaging |
Het |
Pold3 |
A |
G |
7: 99,749,618 (GRCm39) |
|
probably benign |
Het |
Psmd5 |
T |
C |
2: 34,747,784 (GRCm39) |
E291G |
probably damaging |
Het |
Ptpn23 |
A |
G |
9: 110,222,781 (GRCm39) |
V92A |
possibly damaging |
Het |
Rab44 |
T |
A |
17: 29,359,490 (GRCm39) |
H559Q |
probably benign |
Het |
Rbm6 |
T |
C |
9: 107,730,051 (GRCm39) |
D199G |
probably damaging |
Het |
Rps18-ps3 |
C |
T |
8: 107,989,754 (GRCm39) |
|
noncoding transcript |
Het |
Septin10 |
T |
C |
10: 59,006,758 (GRCm39) |
T93A |
probably benign |
Het |
Slmap |
T |
C |
14: 26,184,865 (GRCm39) |
T111A |
probably damaging |
Het |
Spata25 |
C |
T |
2: 164,670,377 (GRCm39) |
M1I |
probably null |
Het |
Spink5 |
T |
A |
18: 44,100,171 (GRCm39) |
C63S |
probably damaging |
Het |
Sycp3 |
T |
C |
10: 88,302,425 (GRCm39) |
|
probably benign |
Het |
Thbs2 |
A |
T |
17: 14,891,716 (GRCm39) |
N940K |
probably benign |
Het |
Tmem106b |
A |
T |
6: 13,081,600 (GRCm39) |
Q169L |
possibly damaging |
Het |
Trpm6 |
G |
T |
19: 18,764,120 (GRCm39) |
C242F |
probably benign |
Het |
Ush2a |
T |
A |
1: 187,999,305 (GRCm39) |
M205K |
probably benign |
Het |
Utp18 |
A |
C |
11: 93,774,617 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tarbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00985:Tarbp1
|
APN |
8 |
127,185,900 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01419:Tarbp1
|
APN |
8 |
127,154,894 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01475:Tarbp1
|
APN |
8 |
127,160,701 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01688:Tarbp1
|
APN |
8 |
127,174,290 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01772:Tarbp1
|
APN |
8 |
127,173,970 (GRCm39) |
splice site |
probably benign |
|
IGL02899:Tarbp1
|
APN |
8 |
127,180,583 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03006:Tarbp1
|
APN |
8 |
127,170,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03273:Tarbp1
|
APN |
8 |
127,180,574 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4280001:Tarbp1
|
UTSW |
8 |
127,157,586 (GRCm39) |
missense |
probably damaging |
0.96 |
R0048:Tarbp1
|
UTSW |
8 |
127,174,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Tarbp1
|
UTSW |
8 |
127,165,667 (GRCm39) |
splice site |
probably benign |
|
R0383:Tarbp1
|
UTSW |
8 |
127,174,223 (GRCm39) |
missense |
probably benign |
0.00 |
R0455:Tarbp1
|
UTSW |
8 |
127,167,612 (GRCm39) |
missense |
probably benign |
0.00 |
R0738:Tarbp1
|
UTSW |
8 |
127,165,540 (GRCm39) |
critical splice donor site |
probably null |
|
R1345:Tarbp1
|
UTSW |
8 |
127,175,069 (GRCm39) |
missense |
probably benign |
0.03 |
R1370:Tarbp1
|
UTSW |
8 |
127,175,069 (GRCm39) |
missense |
probably benign |
0.03 |
R1617:Tarbp1
|
UTSW |
8 |
127,171,007 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1628:Tarbp1
|
UTSW |
8 |
127,157,599 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1702:Tarbp1
|
UTSW |
8 |
127,154,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R1873:Tarbp1
|
UTSW |
8 |
127,173,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R2018:Tarbp1
|
UTSW |
8 |
127,154,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Tarbp1
|
UTSW |
8 |
127,154,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Tarbp1
|
UTSW |
8 |
127,174,333 (GRCm39) |
splice site |
probably null |
|
R2877:Tarbp1
|
UTSW |
8 |
127,154,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R3008:Tarbp1
|
UTSW |
8 |
127,174,160 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3875:Tarbp1
|
UTSW |
8 |
127,165,538 (GRCm39) |
splice site |
probably benign |
|
R3905:Tarbp1
|
UTSW |
8 |
127,154,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Tarbp1
|
UTSW |
8 |
127,167,510 (GRCm39) |
missense |
probably benign |
0.00 |
R4420:Tarbp1
|
UTSW |
8 |
127,173,819 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4570:Tarbp1
|
UTSW |
8 |
127,178,972 (GRCm39) |
missense |
probably benign |
0.00 |
R4610:Tarbp1
|
UTSW |
8 |
127,201,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Tarbp1
|
UTSW |
8 |
127,173,934 (GRCm39) |
missense |
probably damaging |
0.96 |
R4802:Tarbp1
|
UTSW |
8 |
127,201,628 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4951:Tarbp1
|
UTSW |
8 |
127,174,184 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4953:Tarbp1
|
UTSW |
8 |
127,174,184 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5254:Tarbp1
|
UTSW |
8 |
127,193,895 (GRCm39) |
missense |
probably damaging |
0.96 |
R5255:Tarbp1
|
UTSW |
8 |
127,155,709 (GRCm39) |
missense |
probably benign |
0.16 |
R5638:Tarbp1
|
UTSW |
8 |
127,177,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Tarbp1
|
UTSW |
8 |
127,174,079 (GRCm39) |
missense |
probably damaging |
0.98 |
R5707:Tarbp1
|
UTSW |
8 |
127,193,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R5896:Tarbp1
|
UTSW |
8 |
127,179,667 (GRCm39) |
missense |
probably benign |
0.05 |
R6087:Tarbp1
|
UTSW |
8 |
127,155,709 (GRCm39) |
missense |
probably benign |
0.00 |
R6117:Tarbp1
|
UTSW |
8 |
127,154,280 (GRCm39) |
missense |
probably benign |
0.00 |
R6132:Tarbp1
|
UTSW |
8 |
127,161,548 (GRCm39) |
missense |
probably benign |
0.17 |
R6168:Tarbp1
|
UTSW |
8 |
127,175,144 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6419:Tarbp1
|
UTSW |
8 |
127,185,783 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6482:Tarbp1
|
UTSW |
8 |
127,177,434 (GRCm39) |
missense |
probably benign |
0.01 |
R6766:Tarbp1
|
UTSW |
8 |
127,174,139 (GRCm39) |
missense |
probably benign |
0.41 |
R6775:Tarbp1
|
UTSW |
8 |
127,163,568 (GRCm39) |
missense |
probably benign |
0.16 |
R6960:Tarbp1
|
UTSW |
8 |
127,155,778 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7054:Tarbp1
|
UTSW |
8 |
127,201,234 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7068:Tarbp1
|
UTSW |
8 |
127,153,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R7454:Tarbp1
|
UTSW |
8 |
127,184,416 (GRCm39) |
missense |
probably benign |
0.19 |
R7519:Tarbp1
|
UTSW |
8 |
127,160,639 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7760:Tarbp1
|
UTSW |
8 |
127,179,546 (GRCm39) |
missense |
not run |
|
R7837:Tarbp1
|
UTSW |
8 |
127,201,300 (GRCm39) |
missense |
probably benign |
0.00 |
R7882:Tarbp1
|
UTSW |
8 |
127,183,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R7982:Tarbp1
|
UTSW |
8 |
127,171,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R8166:Tarbp1
|
UTSW |
8 |
127,153,867 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8517:Tarbp1
|
UTSW |
8 |
127,170,934 (GRCm39) |
missense |
probably benign |
0.29 |
R8838:Tarbp1
|
UTSW |
8 |
127,177,569 (GRCm39) |
splice site |
probably benign |
|
R8880:Tarbp1
|
UTSW |
8 |
127,198,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R9061:Tarbp1
|
UTSW |
8 |
127,173,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R9123:Tarbp1
|
UTSW |
8 |
127,174,202 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9125:Tarbp1
|
UTSW |
8 |
127,174,202 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9364:Tarbp1
|
UTSW |
8 |
127,177,462 (GRCm39) |
missense |
probably benign |
0.01 |
R9474:Tarbp1
|
UTSW |
8 |
127,155,779 (GRCm39) |
missense |
probably benign |
0.44 |
R9670:Tarbp1
|
UTSW |
8 |
127,183,262 (GRCm39) |
missense |
probably null |
1.00 |
|