Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acy3 |
T |
A |
19: 4,037,758 (GRCm39) |
Y88* |
probably null |
Het |
AI606181 |
T |
A |
19: 41,582,076 (GRCm39) |
I82N |
unknown |
Het |
Akap1 |
T |
C |
11: 88,729,808 (GRCm39) |
Y638C |
probably damaging |
Het |
Angpt1 |
T |
C |
15: 42,323,121 (GRCm39) |
N383D |
probably benign |
Het |
Ank |
T |
C |
15: 27,571,742 (GRCm39) |
|
probably null |
Het |
Aoc1 |
C |
T |
6: 48,882,750 (GRCm39) |
Q209* |
probably null |
Het |
Apol7c |
A |
T |
15: 77,409,875 (GRCm39) |
L357* |
probably null |
Het |
Atxn2l |
A |
G |
7: 126,092,373 (GRCm39) |
L958P |
probably damaging |
Het |
Cab39l |
T |
A |
14: 59,734,395 (GRCm39) |
|
probably null |
Het |
Cdk5rap2 |
A |
G |
4: 70,295,024 (GRCm39) |
|
probably null |
Het |
Cdkn3 |
T |
C |
14: 47,008,918 (GRCm39) |
S204P |
unknown |
Het |
Cds2 |
T |
C |
2: 132,146,400 (GRCm39) |
|
probably null |
Het |
Cideb |
C |
T |
14: 55,992,017 (GRCm39) |
R179H |
probably benign |
Het |
Cped1 |
A |
G |
6: 22,254,625 (GRCm39) |
Q1006R |
probably damaging |
Het |
Csmd2 |
A |
G |
4: 128,350,572 (GRCm39) |
Y1547C |
|
Het |
Dicer1 |
A |
G |
12: 104,675,108 (GRCm39) |
L718S |
probably damaging |
Het |
Dnaaf9 |
C |
A |
2: 130,648,708 (GRCm39) |
R258L |
unknown |
Het |
Dyrk2 |
T |
C |
10: 118,696,136 (GRCm39) |
H374R |
possibly damaging |
Het |
Edem2 |
A |
T |
2: 155,552,886 (GRCm39) |
Y283N |
probably benign |
Het |
Ero1b |
A |
T |
13: 12,615,203 (GRCm39) |
S345C |
possibly damaging |
Het |
Fam83g |
T |
C |
11: 61,593,342 (GRCm39) |
V292A |
possibly damaging |
Het |
Farp2 |
A |
G |
1: 93,507,841 (GRCm39) |
D513G |
possibly damaging |
Het |
Fbxl5 |
A |
G |
5: 43,915,562 (GRCm39) |
W617R |
probably benign |
Het |
Fzd7 |
G |
A |
1: 59,522,443 (GRCm39) |
V109M |
probably damaging |
Het |
Gbp5 |
A |
T |
3: 142,226,898 (GRCm39) |
H583L |
probably benign |
Het |
Gm10306 |
T |
A |
4: 94,445,032 (GRCm39) |
L84M |
unknown |
Het |
Gsap |
A |
G |
5: 21,391,433 (GRCm39) |
T25A |
probably benign |
Het |
Hectd4 |
G |
T |
5: 121,467,136 (GRCm39) |
R2466L |
possibly damaging |
Het |
Ide |
C |
A |
19: 37,268,184 (GRCm39) |
C557F |
|
Het |
Ift70a2 |
A |
T |
2: 75,806,540 (GRCm39) |
Y657* |
probably null |
Het |
Igdcc4 |
T |
A |
9: 65,042,750 (GRCm39) |
C1234* |
probably null |
Het |
Ints4 |
A |
G |
7: 97,179,507 (GRCm39) |
I701V |
probably benign |
Het |
Kalrn |
T |
A |
16: 33,996,792 (GRCm39) |
I1467F |
possibly damaging |
Het |
Kcnip3 |
C |
A |
2: 127,363,256 (GRCm39) |
R2M |
unknown |
Het |
Kcnrg |
A |
T |
14: 61,845,531 (GRCm39) |
E190D |
unknown |
Het |
Klk13 |
T |
C |
7: 43,370,841 (GRCm39) |
L131P |
probably damaging |
Het |
Lhcgr |
A |
T |
17: 89,099,359 (GRCm39) |
L14Q |
possibly damaging |
Het |
Mdm4 |
A |
T |
1: 132,938,853 (GRCm39) |
D80E |
probably damaging |
Het |
Mib2 |
G |
T |
4: 155,742,350 (GRCm39) |
Q311K |
probably damaging |
Het |
Msantd5f9 |
G |
T |
4: 73,835,808 (GRCm39) |
L219M |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,452,773 (GRCm39) |
S1703T |
probably damaging |
Het |
Naip6 |
A |
T |
13: 100,452,011 (GRCm39) |
C200* |
probably null |
Het |
Ncapd3 |
T |
A |
9: 26,961,655 (GRCm39) |
I361N |
probably damaging |
Het |
Nom1 |
A |
G |
5: 29,640,451 (GRCm39) |
E259G |
probably benign |
Het |
Or10j5 |
T |
A |
1: 172,784,673 (GRCm39) |
F104I |
probably damaging |
Het |
Or51v14 |
A |
G |
7: 103,261,089 (GRCm39) |
L157P |
probably damaging |
Het |
Ranbp6 |
T |
C |
19: 29,789,462 (GRCm39) |
T297A |
possibly damaging |
Het |
Rap1gap |
T |
A |
4: 137,455,851 (GRCm39) |
C722* |
probably null |
Het |
Ribc2 |
A |
G |
15: 85,019,733 (GRCm39) |
K172E |
probably benign |
Het |
Scamp5 |
C |
A |
9: 57,354,423 (GRCm39) |
W77L |
probably damaging |
Het |
Scin |
T |
A |
12: 40,130,957 (GRCm39) |
K319* |
probably null |
Het |
Sec16a |
G |
T |
2: 26,329,780 (GRCm39) |
T745K |
probably damaging |
Het |
Slc15a2 |
G |
A |
16: 36,578,173 (GRCm39) |
A403V |
probably benign |
Het |
Slco6c1 |
A |
G |
1: 97,053,466 (GRCm39) |
V145A |
probably benign |
Het |
Sncaip |
C |
T |
18: 53,048,416 (GRCm39) |
H951Y |
probably benign |
Het |
Spem1 |
A |
G |
11: 69,712,630 (GRCm39) |
|
probably null |
Het |
Spen |
C |
T |
4: 141,206,446 (GRCm39) |
R727Q |
unknown |
Het |
Thra |
T |
C |
11: 98,654,544 (GRCm39) |
S305P |
probably damaging |
Het |
Tlr1 |
A |
G |
5: 65,084,067 (GRCm39) |
V170A |
probably damaging |
Het |
Tmem260 |
T |
A |
14: 48,742,786 (GRCm39) |
C388* |
probably null |
Het |
Tmem60 |
T |
A |
5: 21,091,619 (GRCm39) |
V128D |
possibly damaging |
Het |
Tpo |
G |
A |
12: 30,142,685 (GRCm39) |
P680S |
probably benign |
Het |
Umodl1 |
A |
G |
17: 31,205,595 (GRCm39) |
E730G |
possibly damaging |
Het |
Vmn2r69 |
T |
C |
7: 85,056,315 (GRCm39) |
T608A |
probably benign |
Het |
Xrra1 |
G |
A |
7: 99,563,456 (GRCm39) |
S481N |
possibly damaging |
Het |
Zc3h4 |
G |
A |
7: 16,162,961 (GRCm39) |
V446I |
unknown |
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 |
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 |
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 |
|