Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
T |
A |
11: 72,089,671 (GRCm39) |
H71L |
possibly damaging |
Het |
Abcb11 |
C |
A |
2: 69,159,662 (GRCm39) |
V10L |
probably benign |
Het |
Abcb9 |
T |
C |
5: 124,200,950 (GRCm39) |
T689A |
probably damaging |
Het |
Adam22 |
A |
G |
5: 8,193,036 (GRCm39) |
|
probably benign |
Het |
Adamts5 |
A |
G |
16: 85,696,614 (GRCm39) |
I181T |
probably benign |
Het |
Adamts9 |
A |
T |
6: 92,857,938 (GRCm39) |
V231D |
probably damaging |
Het |
Angptl6 |
C |
T |
9: 20,787,823 (GRCm39) |
V197M |
probably damaging |
Het |
Atp6v1c1 |
T |
C |
15: 38,677,772 (GRCm39) |
V99A |
probably benign |
Het |
Cacna2d3 |
A |
G |
14: 29,189,906 (GRCm39) |
V110A |
probably benign |
Het |
Ccdc32 |
A |
G |
2: 118,849,648 (GRCm39) |
|
probably benign |
Het |
Cela3b |
T |
C |
4: 137,155,841 (GRCm39) |
H22R |
probably benign |
Het |
Cep44 |
T |
C |
8: 56,994,008 (GRCm39) |
T190A |
possibly damaging |
Het |
Chsy1 |
T |
C |
7: 65,821,435 (GRCm39) |
C557R |
probably damaging |
Het |
Cntd1 |
A |
G |
11: 101,178,324 (GRCm39) |
T308A |
probably damaging |
Het |
Cutal |
T |
C |
2: 34,775,878 (GRCm39) |
|
probably benign |
Het |
Dipk1b |
A |
G |
2: 26,524,878 (GRCm39) |
T93A |
probably benign |
Het |
Dna2 |
A |
G |
10: 62,792,768 (GRCm39) |
D261G |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,342,911 (GRCm39) |
S1418R |
probably benign |
Het |
Dnpep |
A |
G |
1: 75,288,422 (GRCm39) |
|
probably benign |
Het |
Dock7 |
A |
T |
4: 98,875,716 (GRCm39) |
Y1075N |
probably benign |
Het |
Eif2s1 |
C |
T |
12: 78,928,012 (GRCm39) |
|
probably benign |
Het |
Ess2 |
T |
C |
16: 17,725,419 (GRCm39) |
Y221C |
probably damaging |
Het |
Fer1l6 |
T |
C |
15: 58,425,573 (GRCm39) |
|
probably null |
Het |
Gm5592 |
T |
C |
7: 40,805,254 (GRCm39) |
|
probably benign |
Het |
Ipp |
A |
G |
4: 116,395,073 (GRCm39) |
Y536C |
probably damaging |
Het |
Krt72 |
T |
C |
15: 101,686,740 (GRCm39) |
E402G |
probably damaging |
Het |
Lamb3 |
T |
C |
1: 193,014,638 (GRCm39) |
L599P |
probably damaging |
Het |
Lingo2 |
T |
A |
4: 35,709,120 (GRCm39) |
T287S |
probably benign |
Het |
Lipo3 |
T |
A |
19: 33,537,025 (GRCm39) |
T232S |
probably benign |
Het |
Lrrc63 |
G |
A |
14: 75,363,550 (GRCm39) |
H194Y |
probably benign |
Het |
Map3k13 |
A |
G |
16: 21,725,274 (GRCm39) |
T416A |
probably benign |
Het |
Mcm3 |
A |
T |
1: 20,875,153 (GRCm39) |
|
probably null |
Het |
Mms22l |
T |
C |
4: 24,517,223 (GRCm39) |
V258A |
probably benign |
Het |
Mrpl46 |
A |
T |
7: 78,432,631 (GRCm39) |
L49* |
probably null |
Het |
Mrs2 |
T |
C |
13: 25,177,742 (GRCm39) |
T369A |
possibly damaging |
Het |
Mtrf1 |
T |
A |
14: 79,656,708 (GRCm39) |
Y403* |
probably null |
Het |
Muc20 |
G |
A |
16: 32,614,850 (GRCm39) |
P176S |
unknown |
Het |
Mup21 |
C |
T |
4: 62,068,964 (GRCm39) |
C9Y |
unknown |
Het |
Mup-ps21 |
A |
T |
4: 61,949,007 (GRCm39) |
|
noncoding transcript |
Het |
Mybph |
T |
G |
1: 134,125,081 (GRCm39) |
|
probably null |
Het |
Mypn |
A |
G |
10: 62,970,702 (GRCm39) |
|
probably benign |
Het |
Nav2 |
T |
C |
7: 49,058,431 (GRCm39) |
S124P |
probably damaging |
Het |
Nrros |
T |
C |
16: 31,962,241 (GRCm39) |
D556G |
probably damaging |
Het |
Numa1 |
A |
C |
7: 101,648,884 (GRCm39) |
I872L |
probably benign |
Het |
Or14c40 |
A |
G |
7: 86,313,544 (GRCm39) |
I225V |
possibly damaging |
Het |
Or2a7 |
C |
T |
6: 43,150,938 (GRCm39) |
T6I |
probably benign |
Het |
Or2h2c |
G |
C |
17: 37,422,347 (GRCm39) |
L176V |
probably benign |
Het |
Or4c11 |
A |
T |
2: 88,695,272 (GRCm39) |
M108L |
probably benign |
Het |
Or5p52 |
T |
A |
7: 107,502,446 (GRCm39) |
I174K |
probably damaging |
Het |
Pcdhb9 |
A |
T |
18: 37,535,308 (GRCm39) |
N434I |
probably damaging |
Het |
Pigq |
A |
T |
17: 26,155,736 (GRCm39) |
|
probably null |
Het |
Psma3 |
G |
A |
12: 71,035,269 (GRCm39) |
|
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,703,975 (GRCm39) |
T1336A |
probably benign |
Het |
Rdh7 |
T |
C |
10: 127,720,598 (GRCm39) |
D258G |
probably benign |
Het |
Serpinb6c |
A |
G |
13: 34,083,252 (GRCm39) |
I54T |
probably damaging |
Het |
Sh2d7 |
A |
T |
9: 54,448,633 (GRCm39) |
Y218F |
probably benign |
Het |
Shfl |
AGAGGAGGAGGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGAGGAGGAGGA |
9: 20,785,013 (GRCm39) |
|
probably benign |
Het |
Slc12a8 |
A |
T |
16: 33,371,274 (GRCm39) |
I137F |
possibly damaging |
Het |
Smarca2 |
T |
C |
19: 26,683,600 (GRCm39) |
V1153A |
possibly damaging |
Het |
Smc6 |
A |
T |
12: 11,339,165 (GRCm39) |
I334L |
probably benign |
Het |
Sorcs1 |
A |
G |
19: 50,230,380 (GRCm39) |
|
probably benign |
Het |
Taar8c |
A |
G |
10: 23,977,401 (GRCm39) |
L137P |
probably damaging |
Het |
Tcam1 |
A |
T |
11: 106,176,252 (GRCm39) |
D326V |
possibly damaging |
Het |
Telo2 |
A |
T |
17: 25,324,797 (GRCm39) |
V461D |
probably benign |
Het |
Tmprss7 |
A |
T |
16: 45,498,325 (GRCm39) |
C351* |
probably null |
Het |
Trim66 |
T |
A |
7: 109,054,199 (GRCm39) |
|
probably benign |
Het |
Ube2d1 |
G |
T |
10: 71,097,940 (GRCm39) |
H32N |
probably benign |
Het |
Ubp1 |
T |
C |
9: 113,793,736 (GRCm39) |
|
probably benign |
Het |
Vma21 |
C |
T |
X: 70,863,763 (GRCm39) |
T81M |
probably damaging |
Het |
Vmn1r113 |
T |
C |
7: 20,521,345 (GRCm39) |
S46P |
probably benign |
Het |
Wars1 |
T |
C |
12: 108,831,944 (GRCm39) |
S374G |
probably benign |
Het |
Wbp1 |
T |
C |
6: 83,096,326 (GRCm39) |
D277G |
possibly damaging |
Het |
Zfp939 |
C |
A |
7: 39,123,209 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Plxna2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00227:Plxna2
|
APN |
1 |
194,326,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00332:Plxna2
|
APN |
1 |
194,472,138 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00392:Plxna2
|
APN |
1 |
194,482,876 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00432:Plxna2
|
APN |
1 |
194,326,404 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00704:Plxna2
|
APN |
1 |
194,433,769 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00737:Plxna2
|
APN |
1 |
194,428,547 (GRCm39) |
splice site |
probably benign |
|
IGL01078:Plxna2
|
APN |
1 |
194,469,001 (GRCm39) |
unclassified |
probably benign |
|
IGL01354:Plxna2
|
APN |
1 |
194,444,743 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01432:Plxna2
|
APN |
1 |
194,326,626 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01459:Plxna2
|
APN |
1 |
194,446,878 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01525:Plxna2
|
APN |
1 |
194,394,619 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01656:Plxna2
|
APN |
1 |
194,472,469 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01825:Plxna2
|
APN |
1 |
194,471,210 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01862:Plxna2
|
APN |
1 |
194,326,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01899:Plxna2
|
APN |
1 |
194,433,796 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01996:Plxna2
|
APN |
1 |
194,482,084 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02123:Plxna2
|
APN |
1 |
194,476,691 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02226:Plxna2
|
APN |
1 |
194,326,732 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02227:Plxna2
|
APN |
1 |
194,434,397 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02415:Plxna2
|
APN |
1 |
194,326,272 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02440:Plxna2
|
APN |
1 |
194,428,458 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02545:Plxna2
|
APN |
1 |
194,468,998 (GRCm39) |
unclassified |
probably benign |
|
IGL02553:Plxna2
|
APN |
1 |
194,433,746 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02882:Plxna2
|
APN |
1 |
194,444,878 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02946:Plxna2
|
APN |
1 |
194,431,617 (GRCm39) |
splice site |
probably benign |
|
IGL03062:Plxna2
|
APN |
1 |
194,444,858 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03095:Plxna2
|
APN |
1 |
194,483,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03293:Plxna2
|
APN |
1 |
194,487,253 (GRCm39) |
missense |
probably damaging |
0.99 |
G1Funyon:Plxna2
|
UTSW |
1 |
194,472,483 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4514001:Plxna2
|
UTSW |
1 |
194,477,245 (GRCm39) |
missense |
probably benign |
0.00 |
R0024:Plxna2
|
UTSW |
1 |
194,326,303 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0040:Plxna2
|
UTSW |
1 |
194,326,204 (GRCm39) |
missense |
probably benign |
0.13 |
R0040:Plxna2
|
UTSW |
1 |
194,326,204 (GRCm39) |
missense |
probably benign |
0.13 |
R0063:Plxna2
|
UTSW |
1 |
194,327,247 (GRCm39) |
missense |
probably benign |
0.00 |
R0063:Plxna2
|
UTSW |
1 |
194,327,247 (GRCm39) |
missense |
probably benign |
0.00 |
R0217:Plxna2
|
UTSW |
1 |
194,326,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Plxna2
|
UTSW |
1 |
194,326,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R0440:Plxna2
|
UTSW |
1 |
194,326,712 (GRCm39) |
nonsense |
probably null |
|
R0505:Plxna2
|
UTSW |
1 |
194,326,656 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0568:Plxna2
|
UTSW |
1 |
194,433,694 (GRCm39) |
missense |
probably benign |
0.00 |
R0674:Plxna2
|
UTSW |
1 |
194,331,783 (GRCm39) |
missense |
probably benign |
0.00 |
R0885:Plxna2
|
UTSW |
1 |
194,326,864 (GRCm39) |
missense |
probably benign |
|
R0898:Plxna2
|
UTSW |
1 |
194,479,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R0940:Plxna2
|
UTSW |
1 |
194,482,863 (GRCm39) |
missense |
probably benign |
0.01 |
R1061:Plxna2
|
UTSW |
1 |
194,326,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R1067:Plxna2
|
UTSW |
1 |
194,462,818 (GRCm39) |
splice site |
probably null |
|
R1222:Plxna2
|
UTSW |
1 |
194,482,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R1345:Plxna2
|
UTSW |
1 |
194,326,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R1363:Plxna2
|
UTSW |
1 |
194,487,247 (GRCm39) |
nonsense |
probably null |
|
R1432:Plxna2
|
UTSW |
1 |
194,449,771 (GRCm39) |
missense |
probably benign |
0.10 |
R1434:Plxna2
|
UTSW |
1 |
194,433,848 (GRCm39) |
splice site |
probably benign |
|
R1597:Plxna2
|
UTSW |
1 |
194,431,614 (GRCm39) |
splice site |
probably benign |
|
R1719:Plxna2
|
UTSW |
1 |
194,326,678 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1778:Plxna2
|
UTSW |
1 |
194,493,278 (GRCm39) |
missense |
probably benign |
0.01 |
R1795:Plxna2
|
UTSW |
1 |
194,488,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R1819:Plxna2
|
UTSW |
1 |
194,472,494 (GRCm39) |
missense |
probably benign |
0.03 |
R1926:Plxna2
|
UTSW |
1 |
194,444,758 (GRCm39) |
missense |
probably benign |
0.02 |
R1966:Plxna2
|
UTSW |
1 |
194,327,008 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1987:Plxna2
|
UTSW |
1 |
194,326,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Plxna2
|
UTSW |
1 |
194,326,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R2034:Plxna2
|
UTSW |
1 |
194,462,902 (GRCm39) |
missense |
probably benign |
0.00 |
R2131:Plxna2
|
UTSW |
1 |
194,327,058 (GRCm39) |
missense |
probably benign |
0.01 |
R2171:Plxna2
|
UTSW |
1 |
194,482,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R2217:Plxna2
|
UTSW |
1 |
194,480,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R2311:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2340:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2342:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2423:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2424:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2425:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2842:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2971:Plxna2
|
UTSW |
1 |
194,480,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R3731:Plxna2
|
UTSW |
1 |
194,471,193 (GRCm39) |
missense |
probably benign |
0.42 |
R3783:Plxna2
|
UTSW |
1 |
194,489,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Plxna2
|
UTSW |
1 |
194,326,925 (GRCm39) |
missense |
probably benign |
|
R3787:Plxna2
|
UTSW |
1 |
194,326,242 (GRCm39) |
missense |
probably benign |
0.10 |
R3845:Plxna2
|
UTSW |
1 |
194,476,098 (GRCm39) |
missense |
probably damaging |
0.96 |
R3927:Plxna2
|
UTSW |
1 |
194,428,465 (GRCm39) |
missense |
probably benign |
0.02 |
R3930:Plxna2
|
UTSW |
1 |
194,477,218 (GRCm39) |
missense |
probably benign |
0.17 |
R3964:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R3980:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4067:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Plxna2
|
UTSW |
1 |
194,462,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R4231:Plxna2
|
UTSW |
1 |
194,326,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R4257:Plxna2
|
UTSW |
1 |
194,327,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R4396:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4397:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4418:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4444:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4446:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4482:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4487:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4489:Plxna2
|
UTSW |
1 |
194,431,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R4571:Plxna2
|
UTSW |
1 |
194,493,296 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4622:Plxna2
|
UTSW |
1 |
194,494,458 (GRCm39) |
missense |
probably benign |
|
R4623:Plxna2
|
UTSW |
1 |
194,494,458 (GRCm39) |
missense |
probably benign |
|
R4684:Plxna2
|
UTSW |
1 |
194,444,902 (GRCm39) |
missense |
probably benign |
0.42 |
R4688:Plxna2
|
UTSW |
1 |
194,326,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R4855:Plxna2
|
UTSW |
1 |
194,480,040 (GRCm39) |
missense |
probably benign |
0.39 |
R4876:Plxna2
|
UTSW |
1 |
194,326,083 (GRCm39) |
missense |
probably benign |
0.02 |
R5161:Plxna2
|
UTSW |
1 |
194,433,712 (GRCm39) |
missense |
probably benign |
|
R5207:Plxna2
|
UTSW |
1 |
194,471,207 (GRCm39) |
missense |
probably benign |
0.19 |
R5479:Plxna2
|
UTSW |
1 |
194,476,181 (GRCm39) |
missense |
probably benign |
|
R5931:Plxna2
|
UTSW |
1 |
194,493,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R6026:Plxna2
|
UTSW |
1 |
194,482,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Plxna2
|
UTSW |
1 |
194,481,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Plxna2
|
UTSW |
1 |
194,476,735 (GRCm39) |
missense |
probably benign |
0.00 |
R6059:Plxna2
|
UTSW |
1 |
194,493,279 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6238:Plxna2
|
UTSW |
1 |
194,472,504 (GRCm39) |
missense |
probably benign |
0.01 |
R6322:Plxna2
|
UTSW |
1 |
194,436,675 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6668:Plxna2
|
UTSW |
1 |
194,492,396 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6709:Plxna2
|
UTSW |
1 |
194,472,074 (GRCm39) |
missense |
probably benign |
0.01 |
R6748:Plxna2
|
UTSW |
1 |
194,476,490 (GRCm39) |
splice site |
probably null |
|
R6838:Plxna2
|
UTSW |
1 |
194,487,222 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6844:Plxna2
|
UTSW |
1 |
194,476,136 (GRCm39) |
missense |
probably benign |
0.08 |
R7069:Plxna2
|
UTSW |
1 |
194,476,212 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7122:Plxna2
|
UTSW |
1 |
194,326,876 (GRCm39) |
nonsense |
probably null |
|
R7145:Plxna2
|
UTSW |
1 |
194,331,830 (GRCm39) |
missense |
probably benign |
0.31 |
R7189:Plxna2
|
UTSW |
1 |
194,483,366 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7207:Plxna2
|
UTSW |
1 |
194,326,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Plxna2
|
UTSW |
1 |
194,394,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R7234:Plxna2
|
UTSW |
1 |
194,488,698 (GRCm39) |
missense |
probably damaging |
0.96 |
R7246:Plxna2
|
UTSW |
1 |
194,326,590 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7255:Plxna2
|
UTSW |
1 |
194,434,411 (GRCm39) |
missense |
probably benign |
0.03 |
R7283:Plxna2
|
UTSW |
1 |
194,327,191 (GRCm39) |
missense |
probably damaging |
0.99 |
R7288:Plxna2
|
UTSW |
1 |
194,479,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Plxna2
|
UTSW |
1 |
194,482,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R7424:Plxna2
|
UTSW |
1 |
194,488,647 (GRCm39) |
missense |
probably damaging |
0.98 |
R7501:Plxna2
|
UTSW |
1 |
194,326,203 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7528:Plxna2
|
UTSW |
1 |
194,494,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Plxna2
|
UTSW |
1 |
194,326,179 (GRCm39) |
missense |
probably benign |
0.25 |
R7532:Plxna2
|
UTSW |
1 |
194,327,127 (GRCm39) |
missense |
probably benign |
0.13 |
R7959:Plxna2
|
UTSW |
1 |
194,493,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R7959:Plxna2
|
UTSW |
1 |
194,476,172 (GRCm39) |
frame shift |
probably null |
|
R7960:Plxna2
|
UTSW |
1 |
194,476,172 (GRCm39) |
frame shift |
probably null |
|
R8261:Plxna2
|
UTSW |
1 |
194,431,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R8301:Plxna2
|
UTSW |
1 |
194,472,483 (GRCm39) |
missense |
probably benign |
0.01 |
R8463:Plxna2
|
UTSW |
1 |
194,326,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R8519:Plxna2
|
UTSW |
1 |
194,476,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R8836:Plxna2
|
UTSW |
1 |
194,479,243 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9010:Plxna2
|
UTSW |
1 |
194,471,217 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9034:Plxna2
|
UTSW |
1 |
194,476,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R9254:Plxna2
|
UTSW |
1 |
194,492,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R9274:Plxna2
|
UTSW |
1 |
194,471,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R9379:Plxna2
|
UTSW |
1 |
194,492,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R9385:Plxna2
|
UTSW |
1 |
194,431,724 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9422:Plxna2
|
UTSW |
1 |
194,326,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:Plxna2
|
UTSW |
1 |
194,326,692 (GRCm39) |
missense |
probably benign |
0.05 |
R9484:Plxna2
|
UTSW |
1 |
194,327,202 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Plxna2
|
UTSW |
1 |
194,326,741 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Plxna2
|
UTSW |
1 |
194,446,847 (GRCm39) |
missense |
probably benign |
0.06 |
Z1088:Plxna2
|
UTSW |
1 |
194,326,749 (GRCm39) |
missense |
possibly damaging |
0.56 |
|