Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
G |
T |
11: 109,837,997 (GRCm39) |
S1085* |
probably null |
Het |
Akap9 |
T |
G |
5: 4,001,705 (GRCm39) |
S94A |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,115,856 (GRCm39) |
N3425K |
probably damaging |
Het |
Anapc7 |
T |
A |
5: 122,578,182 (GRCm39) |
I389N |
probably benign |
Het |
Aqp7 |
G |
A |
4: 41,045,321 (GRCm39) |
R20* |
probably null |
Het |
Cacna1h |
C |
T |
17: 25,602,457 (GRCm39) |
G1524R |
probably damaging |
Het |
Cacng4 |
T |
C |
11: 107,685,196 (GRCm39) |
Y32C |
probably damaging |
Het |
Cep120 |
A |
C |
18: 53,847,839 (GRCm39) |
S673R |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,135,986 (GRCm39) |
E19G |
possibly damaging |
Het |
Cpxm2 |
C |
T |
7: 131,661,540 (GRCm39) |
V416I |
probably benign |
Het |
Dapk1 |
A |
G |
13: 60,874,424 (GRCm39) |
T427A |
probably benign |
Het |
Ecm1 |
A |
T |
3: 95,641,586 (GRCm39) |
D549E |
probably benign |
Het |
Efemp1 |
T |
A |
11: 28,871,428 (GRCm39) |
N342K |
probably damaging |
Het |
Erc2 |
T |
C |
14: 27,993,526 (GRCm39) |
|
probably benign |
Het |
Fhip2b |
C |
T |
14: 70,825,130 (GRCm39) |
R402H |
probably benign |
Het |
Galnt13 |
T |
C |
2: 54,747,926 (GRCm39) |
V269A |
probably damaging |
Het |
Gm6465 |
T |
G |
5: 11,899,020 (GRCm39) |
L171R |
probably damaging |
Het |
Gpatch1 |
A |
G |
7: 34,994,703 (GRCm39) |
V521A |
probably benign |
Het |
Heatr5b |
A |
T |
17: 79,103,914 (GRCm39) |
V1087E |
possibly damaging |
Het |
Ikzf2 |
A |
T |
1: 69,578,057 (GRCm39) |
V484D |
probably damaging |
Het |
Ints4 |
T |
A |
7: 97,190,360 (GRCm39) |
V953E |
probably damaging |
Het |
Iqce |
T |
C |
5: 140,685,480 (GRCm39) |
D15G |
possibly damaging |
Het |
Kif3a |
T |
A |
11: 53,461,368 (GRCm39) |
N4K |
possibly damaging |
Het |
Lrch4 |
A |
T |
5: 137,635,271 (GRCm39) |
I254F |
probably damaging |
Het |
Ly75 |
A |
T |
2: 60,129,516 (GRCm39) |
V1623D |
probably damaging |
Het |
Mapt |
T |
A |
11: 104,180,828 (GRCm39) |
|
probably benign |
Het |
Mast1 |
A |
T |
8: 85,639,875 (GRCm39) |
|
probably null |
Het |
Mcc |
G |
T |
18: 44,892,363 (GRCm39) |
Q84K |
probably benign |
Het |
Mgat4f |
G |
A |
1: 134,318,349 (GRCm39) |
V374I |
probably benign |
Het |
Mtfr2 |
G |
A |
10: 20,224,149 (GRCm39) |
V28M |
probably benign |
Het |
Myh8 |
T |
A |
11: 67,180,520 (GRCm39) |
Y585* |
probably null |
Het |
Napsa |
T |
C |
7: 44,231,917 (GRCm39) |
V202A |
probably damaging |
Het |
Nsd2 |
A |
G |
5: 34,001,080 (GRCm39) |
K199R |
probably null |
Het |
Ntpcr |
C |
T |
8: 126,462,837 (GRCm39) |
A18V |
probably benign |
Het |
Or2aj4 |
A |
T |
16: 19,385,426 (GRCm39) |
M69K |
probably damaging |
Het |
Or2g25 |
G |
T |
17: 37,970,368 (GRCm39) |
N285K |
probably damaging |
Het |
Or56b35 |
T |
A |
7: 104,963,439 (GRCm39) |
I76N |
probably damaging |
Het |
Or5g9 |
G |
T |
2: 85,552,472 (GRCm39) |
C241F |
probably damaging |
Het |
Or8b9 |
A |
G |
9: 37,766,477 (GRCm39) |
D121G |
probably damaging |
Het |
Os9 |
A |
G |
10: 126,935,573 (GRCm39) |
V299A |
probably benign |
Het |
Pcdhb7 |
T |
C |
18: 37,476,915 (GRCm39) |
S684P |
possibly damaging |
Het |
Phf19 |
A |
C |
2: 34,787,067 (GRCm39) |
|
probably null |
Het |
Pkd1l3 |
G |
A |
8: 110,357,908 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
A |
G |
1: 20,429,134 (GRCm39) |
I2422T |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,762,038 (GRCm39) |
C459* |
probably null |
Het |
Ptk6 |
T |
C |
2: 180,841,433 (GRCm39) |
S159G |
probably benign |
Het |
Rhd |
T |
C |
4: 134,617,650 (GRCm39) |
I329T |
possibly damaging |
Het |
Scfd1 |
A |
G |
12: 51,492,494 (GRCm39) |
Y601C |
probably damaging |
Het |
Shroom3 |
T |
C |
5: 93,110,148 (GRCm39) |
S1753P |
probably damaging |
Het |
Slc8a1 |
A |
C |
17: 81,749,630 (GRCm39) |
|
probably null |
Het |
Spg7 |
T |
A |
8: 123,803,669 (GRCm39) |
L233Q |
probably damaging |
Het |
Strip1 |
C |
A |
3: 107,529,198 (GRCm39) |
R353L |
probably damaging |
Het |
Ubr1 |
T |
C |
2: 120,764,823 (GRCm39) |
N544D |
possibly damaging |
Het |
Ubr4 |
A |
G |
4: 139,204,469 (GRCm39) |
T4794A |
possibly damaging |
Het |
Usp24 |
A |
G |
4: 106,266,095 (GRCm39) |
|
probably benign |
Het |
Vmn1r193 |
A |
T |
13: 22,403,984 (GRCm39) |
C3S |
probably benign |
Het |
Yju2b |
G |
T |
8: 84,987,163 (GRCm39) |
|
probably benign |
Het |
Zdhhc5 |
C |
T |
2: 84,520,836 (GRCm39) |
R447H |
probably benign |
Het |
Zfp202 |
A |
G |
9: 40,123,124 (GRCm39) |
I629V |
probably benign |
Het |
Zfp462 |
T |
A |
4: 55,023,441 (GRCm39) |
C990S |
probably damaging |
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 |
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 |
R0669:Plxna2
|
UTSW |
1 |
194,471,145 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|