Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
A |
C |
11: 109,974,130 (GRCm39) |
|
probably benign |
Het |
Abcb11 |
G |
T |
2: 69,117,956 (GRCm39) |
P474H |
probably damaging |
Het |
Actn1 |
T |
C |
12: 80,218,537 (GRCm39) |
N749S |
probably benign |
Het |
Atf7ip2 |
T |
A |
16: 10,059,401 (GRCm39) |
|
probably null |
Het |
Brinp3 |
A |
T |
1: 146,776,878 (GRCm39) |
T442S |
probably benign |
Het |
Cdh20 |
A |
G |
1: 110,065,826 (GRCm39) |
N700S |
probably benign |
Het |
Cntn4 |
T |
A |
6: 106,414,865 (GRCm39) |
V132E |
probably damaging |
Het |
Dlc1 |
G |
T |
8: 37,317,345 (GRCm39) |
S443R |
probably benign |
Het |
Evi2b |
T |
A |
11: 79,406,893 (GRCm39) |
K227N |
probably damaging |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gstm3 |
T |
C |
3: 107,874,973 (GRCm39) |
E93G |
probably damaging |
Het |
Hemgn |
T |
C |
4: 46,396,057 (GRCm39) |
Y393C |
probably damaging |
Het |
Hepacam2 |
T |
A |
6: 3,487,117 (GRCm39) |
Y4F |
probably benign |
Het |
Hipk1 |
T |
C |
3: 103,651,320 (GRCm39) |
I1148V |
possibly damaging |
Het |
Katnip |
A |
G |
7: 125,453,777 (GRCm39) |
T1165A |
probably benign |
Het |
Kl |
A |
T |
5: 150,912,402 (GRCm39) |
D717V |
probably damaging |
Het |
Mmp14 |
T |
C |
14: 54,675,053 (GRCm39) |
|
probably benign |
Het |
Nlrp1b |
T |
G |
11: 71,072,233 (GRCm39) |
T537P |
probably damaging |
Het |
Or5k3 |
T |
C |
16: 58,969,827 (GRCm39) |
S205P |
probably benign |
Het |
Or8k33 |
A |
G |
2: 86,383,793 (GRCm39) |
V225A |
probably benign |
Het |
Pcnx3 |
A |
G |
19: 5,727,691 (GRCm39) |
V1031A |
probably benign |
Het |
Plk2 |
A |
G |
13: 110,535,588 (GRCm39) |
D470G |
possibly damaging |
Het |
Ppa1 |
G |
A |
10: 61,501,215 (GRCm39) |
V161M |
probably benign |
Het |
Psmd6 |
A |
T |
14: 14,116,169 (GRCm38) |
S140T |
probably benign |
Het |
Ptprm |
A |
G |
17: 67,353,158 (GRCm39) |
|
probably benign |
Het |
Ranbp17 |
T |
C |
11: 33,278,520 (GRCm39) |
T116A |
possibly damaging |
Het |
Reps1 |
A |
G |
10: 17,969,584 (GRCm39) |
N229S |
probably benign |
Het |
Rfx3 |
A |
T |
19: 27,808,129 (GRCm39) |
Y205N |
probably damaging |
Het |
Robo1 |
A |
T |
16: 72,759,114 (GRCm39) |
I376F |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,805,249 (GRCm39) |
I872F |
probably damaging |
Het |
Selenop |
C |
T |
15: 3,308,750 (GRCm39) |
T234M |
probably benign |
Het |
Sgip1 |
T |
C |
4: 102,823,439 (GRCm39) |
Y707H |
probably damaging |
Het |
Strap |
A |
G |
6: 137,718,333 (GRCm39) |
I146V |
probably benign |
Het |
Tcim |
A |
T |
8: 24,928,892 (GRCm39) |
H7Q |
probably benign |
Het |
Thada |
G |
T |
17: 84,530,194 (GRCm39) |
T1725N |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r84 |
A |
G |
10: 130,221,755 (GRCm39) |
C822R |
probably damaging |
Het |
|
Other mutations in Prrc2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00482:Prrc2a
|
APN |
17 |
35,373,959 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01083:Prrc2a
|
APN |
17 |
35,375,177 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01394:Prrc2a
|
APN |
17 |
35,372,080 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01618:Prrc2a
|
APN |
17 |
35,368,529 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01700:Prrc2a
|
APN |
17 |
35,369,643 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02407:Prrc2a
|
APN |
17 |
35,379,480 (GRCm39) |
missense |
unknown |
|
IGL02683:Prrc2a
|
APN |
17 |
35,374,969 (GRCm39) |
missense |
probably benign |
0.00 |
R0145:Prrc2a
|
UTSW |
17 |
35,374,796 (GRCm39) |
missense |
probably benign |
|
R0309:Prrc2a
|
UTSW |
17 |
35,369,891 (GRCm39) |
splice site |
probably benign |
|
R0441:Prrc2a
|
UTSW |
17 |
35,368,664 (GRCm39) |
splice site |
probably benign |
|
R0617:Prrc2a
|
UTSW |
17 |
35,372,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Prrc2a
|
UTSW |
17 |
35,375,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R1351:Prrc2a
|
UTSW |
17 |
35,376,863 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1432:Prrc2a
|
UTSW |
17 |
35,372,888 (GRCm39) |
splice site |
probably benign |
|
R1490:Prrc2a
|
UTSW |
17 |
35,372,230 (GRCm39) |
missense |
probably benign |
|
R1643:Prrc2a
|
UTSW |
17 |
35,375,930 (GRCm39) |
missense |
probably damaging |
0.99 |
R1734:Prrc2a
|
UTSW |
17 |
35,369,683 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1869:Prrc2a
|
UTSW |
17 |
35,372,284 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1937:Prrc2a
|
UTSW |
17 |
35,376,884 (GRCm39) |
missense |
probably damaging |
0.99 |
R1995:Prrc2a
|
UTSW |
17 |
35,376,405 (GRCm39) |
missense |
probably damaging |
0.98 |
R2257:Prrc2a
|
UTSW |
17 |
35,380,044 (GRCm39) |
missense |
unknown |
|
R2270:Prrc2a
|
UTSW |
17 |
35,368,512 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3940:Prrc2a
|
UTSW |
17 |
35,376,474 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3973:Prrc2a
|
UTSW |
17 |
35,376,908 (GRCm39) |
missense |
probably damaging |
0.99 |
R4569:Prrc2a
|
UTSW |
17 |
35,377,473 (GRCm39) |
missense |
unknown |
|
R4655:Prrc2a
|
UTSW |
17 |
35,374,590 (GRCm39) |
missense |
probably benign |
0.00 |
R4792:Prrc2a
|
UTSW |
17 |
35,375,463 (GRCm39) |
missense |
probably damaging |
0.96 |
R4797:Prrc2a
|
UTSW |
17 |
35,369,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Prrc2a
|
UTSW |
17 |
35,369,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Prrc2a
|
UTSW |
17 |
35,369,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Prrc2a
|
UTSW |
17 |
35,368,974 (GRCm39) |
missense |
probably benign |
0.11 |
R5129:Prrc2a
|
UTSW |
17 |
35,379,154 (GRCm39) |
missense |
unknown |
|
R5155:Prrc2a
|
UTSW |
17 |
35,379,067 (GRCm39) |
splice site |
probably null |
|
R5210:Prrc2a
|
UTSW |
17 |
35,372,596 (GRCm39) |
missense |
probably damaging |
0.99 |
R5308:Prrc2a
|
UTSW |
17 |
35,380,023 (GRCm39) |
missense |
unknown |
|
R5474:Prrc2a
|
UTSW |
17 |
35,378,189 (GRCm39) |
missense |
unknown |
|
R5775:Prrc2a
|
UTSW |
17 |
35,377,463 (GRCm39) |
missense |
unknown |
|
R5934:Prrc2a
|
UTSW |
17 |
35,369,060 (GRCm39) |
missense |
probably damaging |
0.98 |
R6057:Prrc2a
|
UTSW |
17 |
35,371,716 (GRCm39) |
missense |
probably benign |
0.00 |
R6291:Prrc2a
|
UTSW |
17 |
35,373,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R6535:Prrc2a
|
UTSW |
17 |
35,381,241 (GRCm39) |
missense |
unknown |
|
R6622:Prrc2a
|
UTSW |
17 |
35,374,396 (GRCm39) |
missense |
probably damaging |
0.98 |
R6887:Prrc2a
|
UTSW |
17 |
35,374,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R6971:Prrc2a
|
UTSW |
17 |
35,378,477 (GRCm39) |
splice site |
probably null |
|
R7026:Prrc2a
|
UTSW |
17 |
35,380,803 (GRCm39) |
missense |
unknown |
|
R7059:Prrc2a
|
UTSW |
17 |
35,376,364 (GRCm39) |
missense |
probably damaging |
0.99 |
R7489:Prrc2a
|
UTSW |
17 |
35,381,330 (GRCm39) |
missense |
unknown |
|
R7502:Prrc2a
|
UTSW |
17 |
35,381,286 (GRCm39) |
missense |
unknown |
|
R7951:Prrc2a
|
UTSW |
17 |
35,379,477 (GRCm39) |
missense |
unknown |
|
R8061:Prrc2a
|
UTSW |
17 |
35,380,162 (GRCm39) |
splice site |
probably benign |
|
R8324:Prrc2a
|
UTSW |
17 |
35,375,960 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8705:Prrc2a
|
UTSW |
17 |
35,372,542 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9016:Prrc2a
|
UTSW |
17 |
35,378,844 (GRCm39) |
missense |
unknown |
|
R9310:Prrc2a
|
UTSW |
17 |
35,374,975 (GRCm39) |
missense |
probably benign |
0.38 |
R9376:Prrc2a
|
UTSW |
17 |
35,369,598 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9645:Prrc2a
|
UTSW |
17 |
35,381,176 (GRCm39) |
critical splice donor site |
probably null |
|
R9703:Prrc2a
|
UTSW |
17 |
35,378,320 (GRCm39) |
missense |
unknown |
|
X0011:Prrc2a
|
UTSW |
17 |
35,374,874 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Prrc2a
|
UTSW |
17 |
35,380,336 (GRCm39) |
missense |
unknown |
|
Z1177:Prrc2a
|
UTSW |
17 |
35,374,676 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Prrc2a
|
UTSW |
17 |
35,373,791 (GRCm39) |
missense |
probably damaging |
0.98 |
|