Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
A |
G |
12: 71,217,361 (GRCm39) |
|
probably null |
Het |
9130401M01Rik |
A |
T |
15: 57,892,256 (GRCm39) |
L117Q |
probably damaging |
Het |
Abcb1b |
A |
G |
5: 8,887,771 (GRCm39) |
K886E |
possibly damaging |
Het |
Acaa2 |
A |
T |
18: 74,920,198 (GRCm39) |
I9F |
probably damaging |
Het |
Acap2 |
A |
T |
16: 30,929,901 (GRCm39) |
S386T |
probably damaging |
Het |
Acsm2 |
A |
T |
7: 119,172,798 (GRCm39) |
I138F |
possibly damaging |
Het |
Agl |
T |
C |
3: 116,540,342 (GRCm39) |
Y1424C |
probably damaging |
Het |
Aoc1l1 |
T |
A |
6: 48,952,588 (GRCm39) |
F171Y |
probably damaging |
Het |
Apc2 |
T |
C |
10: 80,148,183 (GRCm39) |
V1079A |
probably benign |
Het |
Arhgef6 |
T |
C |
X: 56,383,922 (GRCm39) |
M5V |
probably benign |
Het |
Armc8 |
C |
T |
9: 99,405,185 (GRCm39) |
|
probably benign |
Het |
Catsperb |
A |
G |
12: 101,588,476 (GRCm39) |
Y953C |
probably damaging |
Het |
Cdk13 |
G |
A |
13: 17,893,001 (GRCm39) |
A720V |
probably damaging |
Het |
Chka |
T |
C |
19: 3,924,809 (GRCm39) |
|
probably benign |
Het |
Clcc1 |
T |
C |
3: 108,575,418 (GRCm39) |
I165T |
probably benign |
Het |
Cndp1 |
G |
A |
18: 84,652,777 (GRCm39) |
|
probably benign |
Het |
Dip2c |
C |
A |
13: 9,603,340 (GRCm39) |
P297Q |
probably damaging |
Het |
Dnah17 |
A |
T |
11: 117,914,153 (GRCm39) |
W4429R |
probably damaging |
Het |
Dram2 |
T |
C |
3: 106,478,082 (GRCm39) |
V138A |
possibly damaging |
Het |
Dus4l |
T |
C |
12: 31,698,770 (GRCm39) |
N78S |
probably benign |
Het |
Dync1h1 |
G |
A |
12: 110,602,943 (GRCm39) |
E2195K |
probably benign |
Het |
Ebf1 |
T |
C |
11: 44,895,533 (GRCm39) |
|
probably benign |
Het |
Epm2a |
T |
A |
10: 11,266,587 (GRCm39) |
Y111N |
probably damaging |
Het |
Gm773 |
T |
C |
X: 55,247,377 (GRCm39) |
T52A |
probably benign |
Het |
Gpam |
C |
A |
19: 55,067,693 (GRCm39) |
M483I |
probably damaging |
Het |
Gpr12 |
T |
C |
5: 146,520,235 (GRCm39) |
H229R |
probably damaging |
Het |
Gpr149 |
T |
C |
3: 62,438,439 (GRCm39) |
T573A |
probably damaging |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Hells |
T |
A |
19: 38,945,628 (GRCm39) |
|
probably null |
Het |
Herc1 |
T |
A |
9: 66,372,751 (GRCm39) |
N3102K |
probably benign |
Het |
Herc3 |
A |
T |
6: 58,893,827 (GRCm39) |
T968S |
possibly damaging |
Het |
Ift88 |
A |
G |
14: 57,674,736 (GRCm39) |
Y69C |
probably benign |
Het |
Incenp |
G |
A |
19: 9,862,890 (GRCm39) |
T388M |
unknown |
Het |
Jrkl |
A |
G |
9: 13,245,337 (GRCm39) |
F108S |
probably benign |
Het |
Khdc1a |
A |
G |
1: 21,420,542 (GRCm39) |
E54G |
possibly damaging |
Het |
Kif6 |
T |
A |
17: 49,927,728 (GRCm39) |
F58L |
probably damaging |
Het |
Klk14 |
T |
C |
7: 43,344,342 (GRCm39) |
S218P |
probably damaging |
Het |
Kmt2e |
T |
C |
5: 23,655,319 (GRCm39) |
M19T |
probably benign |
Het |
Llgl1 |
G |
T |
11: 60,599,380 (GRCm39) |
G454C |
probably damaging |
Het |
Lyrm4 |
A |
G |
13: 36,276,898 (GRCm39) |
V33A |
probably benign |
Het |
Mcam |
C |
T |
9: 44,052,588 (GRCm39) |
R606C |
probably damaging |
Het |
Mgam |
T |
A |
6: 40,733,301 (GRCm39) |
M692K |
probably damaging |
Het |
Mmp28 |
C |
T |
11: 83,333,765 (GRCm39) |
R392H |
probably damaging |
Het |
Mpdz |
G |
A |
4: 81,210,788 (GRCm39) |
T1699M |
probably damaging |
Het |
Mrps11 |
T |
C |
7: 78,433,310 (GRCm39) |
|
probably benign |
Het |
Mrtfb |
A |
G |
16: 13,218,866 (GRCm39) |
N504S |
probably benign |
Het |
Msmo1 |
A |
G |
8: 65,180,650 (GRCm39) |
|
probably benign |
Het |
Mst1 |
A |
G |
9: 107,961,403 (GRCm39) |
E571G |
probably benign |
Het |
Myh14 |
T |
C |
7: 44,265,723 (GRCm39) |
E1585G |
probably damaging |
Het |
Myrfl |
A |
G |
10: 116,613,332 (GRCm39) |
C824R |
probably damaging |
Het |
Ncapd3 |
C |
T |
9: 26,981,168 (GRCm39) |
|
probably benign |
Het |
Nlrp4a |
G |
GGTTCTTC |
7: 26,163,622 (GRCm39) |
|
probably null |
Het |
Nos1 |
C |
T |
5: 118,087,684 (GRCm39) |
|
probably benign |
Het |
Notch3 |
T |
C |
17: 32,383,198 (GRCm39) |
S47G |
probably benign |
Het |
Npsr1 |
A |
G |
9: 24,221,371 (GRCm39) |
Y122C |
probably damaging |
Het |
Or10ak12 |
T |
C |
4: 118,666,435 (GRCm39) |
M209V |
probably benign |
Het |
Or1j11 |
C |
T |
2: 36,311,655 (GRCm39) |
L82F |
probably damaging |
Het |
Or5a1 |
G |
T |
19: 12,097,603 (GRCm39) |
R158S |
possibly damaging |
Het |
Or6c1b |
C |
T |
10: 129,272,807 (GRCm39) |
T42I |
probably damaging |
Het |
Or6k2 |
T |
A |
1: 173,986,483 (GRCm39) |
V48E |
possibly damaging |
Het |
Or8b9 |
T |
A |
9: 37,766,548 (GRCm39) |
L145M |
possibly damaging |
Het |
Otog |
G |
T |
7: 45,950,007 (GRCm39) |
V2490F |
probably damaging |
Het |
Pibf1 |
T |
C |
14: 99,350,425 (GRCm39) |
V191A |
probably benign |
Het |
Pip |
A |
G |
6: 41,826,852 (GRCm39) |
M66V |
probably benign |
Het |
Prkca |
A |
T |
11: 107,830,346 (GRCm39) |
V248E |
probably benign |
Het |
Prmt7 |
T |
A |
8: 106,963,916 (GRCm39) |
L253* |
probably null |
Het |
Prrc2a |
G |
T |
17: 35,372,888 (GRCm39) |
|
probably benign |
Het |
Rasgrf1 |
A |
G |
9: 89,894,853 (GRCm39) |
D1091G |
probably benign |
Het |
Rbm7 |
C |
A |
9: 48,401,245 (GRCm39) |
G161V |
probably benign |
Het |
Scn1a |
A |
T |
2: 66,152,773 (GRCm39) |
I736N |
probably damaging |
Het |
Skint6 |
A |
G |
4: 112,726,721 (GRCm39) |
|
probably benign |
Het |
Slc22a2 |
C |
T |
17: 12,803,195 (GRCm39) |
H10Y |
possibly damaging |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Stam2 |
A |
G |
2: 52,604,821 (GRCm39) |
|
probably benign |
Het |
Stk40 |
T |
C |
4: 126,030,626 (GRCm39) |
L282P |
probably damaging |
Het |
Tas2r110 |
A |
G |
6: 132,845,331 (GRCm39) |
N121D |
probably damaging |
Het |
Tbc1d32 |
A |
G |
10: 55,893,758 (GRCm39) |
Y1272H |
probably damaging |
Het |
Thoc2l |
T |
C |
5: 104,665,970 (GRCm39) |
F164S |
probably damaging |
Het |
Tmem131l |
T |
C |
3: 83,836,021 (GRCm39) |
D696G |
probably damaging |
Het |
Trdmt1 |
T |
C |
2: 13,524,657 (GRCm39) |
Y266C |
probably damaging |
Het |
Trim5 |
G |
T |
7: 103,928,726 (GRCm39) |
H72N |
probably benign |
Het |
Trim5 |
A |
C |
7: 103,928,728 (GRCm39) |
L71R |
probably benign |
Het |
Twf2 |
T |
A |
9: 106,092,012 (GRCm39) |
|
probably benign |
Het |
Ubap2l |
T |
C |
3: 89,926,635 (GRCm39) |
T580A |
probably benign |
Het |
Ugt1a10 |
C |
T |
1: 88,143,982 (GRCm39) |
R201C |
probably damaging |
Het |
Unc5a |
A |
G |
13: 55,152,285 (GRCm39) |
|
probably benign |
Het |
Vmn2r85 |
T |
C |
10: 130,261,155 (GRCm39) |
N394S |
possibly damaging |
Het |
Wrn |
A |
T |
8: 33,809,169 (GRCm39) |
|
probably benign |
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 |
|
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 |
|