Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
T |
C |
15: 64,659,191 (GRCm39) |
D533G |
probably benign |
Het |
Adgb |
A |
G |
10: 10,283,298 (GRCm39) |
V136A |
possibly damaging |
Het |
Aggf1 |
A |
G |
13: 95,492,917 (GRCm39) |
V564A |
probably damaging |
Het |
Atp1a2 |
T |
C |
1: 172,112,186 (GRCm39) |
T570A |
probably benign |
Het |
Bicdl2 |
A |
G |
17: 23,887,105 (GRCm39) |
Q464R |
probably damaging |
Het |
Cacng5 |
C |
T |
11: 107,772,531 (GRCm39) |
V106I |
probably benign |
Het |
Chd8 |
C |
A |
14: 52,458,877 (GRCm39) |
R792L |
probably damaging |
Het |
Crybg2 |
A |
T |
4: 133,802,755 (GRCm39) |
I844F |
possibly damaging |
Het |
Dock4 |
G |
A |
12: 40,838,380 (GRCm39) |
|
probably benign |
Het |
Ergic2 |
T |
C |
6: 148,096,769 (GRCm39) |
T166A |
probably benign |
Het |
Flrt2 |
A |
T |
12: 95,747,121 (GRCm39) |
R486S |
probably benign |
Het |
Flt3 |
T |
C |
5: 147,291,680 (GRCm39) |
Y590C |
probably damaging |
Het |
Fubp1 |
A |
G |
3: 151,927,871 (GRCm39) |
E441G |
probably damaging |
Het |
Gfpt1 |
A |
G |
6: 87,031,678 (GRCm39) |
S107G |
probably damaging |
Het |
Klra9 |
A |
G |
6: 130,166,729 (GRCm39) |
L45P |
possibly damaging |
Het |
Mfsd5 |
A |
G |
15: 102,189,525 (GRCm39) |
Y299C |
probably damaging |
Het |
Myo5b |
T |
A |
18: 74,866,974 (GRCm39) |
|
probably benign |
Het |
Obscn |
G |
A |
11: 58,926,919 (GRCm39) |
T5532M |
probably damaging |
Het |
Or5ac25 |
G |
A |
16: 59,182,198 (GRCm39) |
P128S |
probably damaging |
Het |
Palld |
A |
G |
8: 61,991,841 (GRCm39) |
S165P |
probably benign |
Het |
Pramel17 |
T |
A |
4: 101,692,729 (GRCm39) |
M424L |
probably benign |
Het |
Prokr1 |
A |
T |
6: 87,565,766 (GRCm39) |
H26Q |
probably benign |
Het |
Rasgrp1 |
A |
G |
2: 117,115,549 (GRCm39) |
W680R |
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,582,191 (GRCm39) |
|
probably benign |
Het |
Sars1 |
A |
G |
3: 108,334,174 (GRCm39) |
L528P |
probably damaging |
Het |
Serpinb3b |
T |
A |
1: 107,085,473 (GRCm39) |
L89F |
possibly damaging |
Het |
Slc38a6 |
T |
C |
12: 73,335,267 (GRCm39) |
V70A |
possibly damaging |
Het |
Son |
G |
A |
16: 91,454,279 (GRCm39) |
E1009K |
probably damaging |
Het |
Thoc3 |
A |
C |
13: 54,615,633 (GRCm39) |
|
probably benign |
Het |
Tlk2 |
T |
A |
11: 105,112,050 (GRCm39) |
C88S |
probably benign |
Het |
Tmem182 |
T |
A |
1: 40,844,977 (GRCm39) |
F21Y |
probably damaging |
Het |
Tmem214 |
G |
A |
5: 31,033,437 (GRCm39) |
V557M |
probably benign |
Het |
Zfp507 |
T |
C |
7: 35,493,463 (GRCm39) |
T527A |
probably benign |
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 |
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 |
IGL01937:Prrc2a
|
APN |
17 |
35,374,567 (GRCm39) |
missense |
possibly damaging |
0.63 |
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 |
|