Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310039H08Rik |
T |
C |
17: 47,083,872 (GRCm39) |
V45A |
probably benign |
Het |
4921509C19Rik |
A |
G |
2: 151,313,791 (GRCm39) |
I629T |
unknown |
Het |
4933402N03Rik |
T |
C |
7: 130,740,413 (GRCm39) |
R268G |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,384,193 (GRCm39) |
R3882* |
probably null |
Het |
Adamts3 |
T |
G |
5: 89,850,866 (GRCm39) |
T558P |
probably damaging |
Het |
Ano2 |
A |
G |
6: 125,767,304 (GRCm39) |
N214S |
probably benign |
Het |
Arhgef4 |
A |
T |
1: 34,850,866 (GRCm39) |
|
probably null |
Het |
Boc |
C |
T |
16: 44,320,743 (GRCm39) |
A306T |
probably benign |
Het |
Capn10 |
T |
C |
1: 92,871,503 (GRCm39) |
F367S |
probably damaging |
Het |
Ccdc6 |
T |
C |
10: 70,025,086 (GRCm39) |
|
probably benign |
Het |
Cobll1 |
G |
T |
2: 64,929,372 (GRCm39) |
S688R |
possibly damaging |
Het |
Cpxm2 |
G |
T |
7: 131,650,767 (GRCm39) |
P631Q |
possibly damaging |
Het |
Cyp2c68 |
A |
G |
19: 39,687,779 (GRCm39) |
V406A |
possibly damaging |
Het |
Cyp4a30b |
T |
A |
4: 115,312,200 (GRCm39) |
Y118N |
probably damaging |
Het |
Dgki |
A |
T |
6: 37,276,781 (GRCm39) |
|
probably benign |
Het |
Disp2 |
A |
G |
2: 118,623,237 (GRCm39) |
N1323S |
probably damaging |
Het |
Dock1 |
T |
A |
7: 134,326,138 (GRCm39) |
Y42* |
probably null |
Het |
Eps8l1 |
C |
A |
7: 4,476,944 (GRCm39) |
P471Q |
probably damaging |
Het |
Fam20a |
A |
C |
11: 109,612,513 (GRCm39) |
L10R |
unknown |
Het |
Fpr-rs4 |
T |
A |
17: 18,242,446 (GRCm39) |
I151K |
probably damaging |
Het |
Gga1 |
C |
A |
15: 78,769,509 (GRCm39) |
P161T |
probably damaging |
Het |
Gm9923 |
T |
A |
10: 72,145,306 (GRCm39) |
Y52* |
probably null |
Het |
Gucy2g |
A |
G |
19: 55,194,688 (GRCm39) |
F910L |
probably damaging |
Het |
H2-T5 |
A |
T |
17: 36,476,750 (GRCm39) |
H241Q |
possibly damaging |
Het |
Helz |
T |
C |
11: 107,539,971 (GRCm39) |
V315A |
probably damaging |
Het |
Hk2 |
T |
C |
6: 82,716,629 (GRCm39) |
Y301C |
probably damaging |
Het |
Htt |
C |
T |
5: 35,010,109 (GRCm39) |
P1521S |
probably damaging |
Het |
Iah1 |
T |
C |
12: 21,366,434 (GRCm39) |
M1T |
probably null |
Het |
Ik |
T |
C |
18: 36,885,467 (GRCm39) |
S287P |
probably damaging |
Het |
Itga1 |
T |
A |
13: 115,185,906 (GRCm39) |
D32V |
probably damaging |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Klk14 |
A |
G |
7: 43,341,392 (GRCm39) |
I15V |
probably benign |
Het |
Kng2 |
T |
C |
16: 22,806,391 (GRCm39) |
I603V |
possibly damaging |
Het |
Lama1 |
T |
C |
17: 68,080,773 (GRCm39) |
I1267T |
possibly damaging |
Het |
Lrp1b |
A |
C |
2: 40,812,316 (GRCm39) |
L2430V |
probably benign |
Het |
Lrrn3 |
T |
G |
12: 41,504,243 (GRCm39) |
K25Q |
possibly damaging |
Het |
Lta4h |
T |
A |
10: 93,304,678 (GRCm39) |
N233K |
probably benign |
Het |
Mapk13 |
T |
C |
17: 28,989,023 (GRCm39) |
I53T |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,666,430 (GRCm39) |
F123L |
probably damaging |
Het |
Myh4 |
G |
C |
11: 67,136,637 (GRCm39) |
D472H |
probably damaging |
Het |
Nipa2 |
A |
T |
7: 55,585,574 (GRCm39) |
N121K |
probably benign |
Het |
Nostrin |
C |
T |
2: 69,014,268 (GRCm39) |
T408M |
probably benign |
Het |
Oosp2 |
C |
T |
19: 11,627,017 (GRCm39) |
R102H |
probably damaging |
Het |
Or1j18 |
A |
G |
2: 36,624,686 (GRCm39) |
M118V |
probably damaging |
Het |
Or4k15b |
T |
C |
14: 50,272,287 (GRCm39) |
D191G |
probably damaging |
Het |
Osgin2 |
T |
A |
4: 16,001,946 (GRCm39) |
I202L |
probably benign |
Het |
Pbld2 |
C |
A |
10: 62,893,476 (GRCm39) |
R271S |
probably damaging |
Het |
Pex6 |
C |
T |
17: 47,023,027 (GRCm39) |
T201I |
probably benign |
Het |
Pilra |
T |
C |
5: 137,833,777 (GRCm39) |
I96M |
probably damaging |
Het |
Pllp |
T |
A |
8: 95,403,906 (GRCm39) |
D47V |
possibly damaging |
Het |
Prkca |
A |
T |
11: 107,852,434 (GRCm39) |
Y100N |
probably damaging |
Het |
Prkg1 |
T |
A |
19: 31,641,579 (GRCm39) |
K35* |
probably null |
Het |
Psmc2 |
A |
G |
5: 22,008,263 (GRCm39) |
D389G |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,331,951 (GRCm39) |
T2387A |
probably damaging |
Het |
Ros1 |
T |
C |
10: 52,005,192 (GRCm39) |
N914S |
probably damaging |
Het |
Ruvbl1 |
C |
A |
6: 88,468,581 (GRCm39) |
T367K |
probably benign |
Het |
Scube2 |
C |
T |
7: 109,409,920 (GRCm39) |
R525H |
probably damaging |
Het |
Sec14l4 |
T |
C |
11: 3,985,200 (GRCm39) |
|
probably null |
Het |
Secisbp2l |
T |
C |
2: 125,587,862 (GRCm39) |
D751G |
probably damaging |
Het |
Setd3 |
T |
C |
12: 108,074,949 (GRCm39) |
D402G |
probably benign |
Het |
Slc15a2 |
T |
A |
16: 36,578,211 (GRCm39) |
K359N |
probably damaging |
Het |
Slc25a21 |
A |
G |
12: 57,243,721 (GRCm39) |
S2P |
probably benign |
Het |
Slfn8 |
A |
T |
11: 82,908,332 (GRCm39) |
H70Q |
probably benign |
Het |
Spef2 |
T |
C |
15: 9,647,576 (GRCm39) |
I944V |
probably benign |
Het |
Spg11 |
A |
G |
2: 121,895,557 (GRCm39) |
F1887S |
probably damaging |
Het |
Sptbn4 |
A |
T |
7: 27,066,160 (GRCm39) |
D649E |
possibly damaging |
Het |
Sptbn4 |
T |
C |
7: 27,063,844 (GRCm39) |
E879G |
probably damaging |
Het |
Stx5a |
C |
A |
19: 8,720,725 (GRCm39) |
R121S |
probably damaging |
Het |
Tbcd |
T |
C |
11: 121,384,597 (GRCm39) |
L26P |
probably damaging |
Het |
Tecpr1 |
T |
C |
5: 144,144,255 (GRCm39) |
D649G |
probably benign |
Het |
Tfam |
A |
G |
10: 71,073,677 (GRCm39) |
S32P |
probably benign |
Het |
Tmt1b |
G |
T |
10: 128,796,571 (GRCm39) |
C79* |
probably null |
Het |
Trmt44 |
C |
T |
5: 35,715,387 (GRCm39) |
R642H |
probably benign |
Het |
Trpm3 |
G |
A |
19: 22,965,145 (GRCm39) |
A1547T |
probably benign |
Het |
Ttll6 |
T |
C |
11: 96,044,003 (GRCm39) |
V519A |
probably benign |
Het |
Umodl1 |
T |
C |
17: 31,217,088 (GRCm39) |
F1107L |
probably benign |
Het |
Usp5 |
A |
T |
6: 124,794,919 (GRCm39) |
V677E |
probably damaging |
Het |
Utp20 |
A |
T |
10: 88,643,307 (GRCm39) |
L605* |
probably null |
Het |
Utrn |
T |
C |
10: 12,620,984 (GRCm39) |
D229G |
probably damaging |
Het |
Uty |
A |
T |
Y: 1,176,502 (GRCm39) |
L178* |
probably null |
Het |
Vmn2r88 |
A |
T |
14: 51,650,791 (GRCm39) |
D168V |
possibly damaging |
Het |
Vps13b |
T |
C |
15: 35,646,324 (GRCm39) |
V1476A |
probably damaging |
Het |
Vps13b |
C |
A |
15: 35,879,967 (GRCm39) |
T3014K |
probably benign |
Het |
Vps13b |
C |
T |
15: 35,841,487 (GRCm39) |
H2506Y |
probably benign |
Het |
Vps37c |
T |
C |
19: 10,690,132 (GRCm39) |
V198A |
probably benign |
Het |
Zfc3h1 |
T |
C |
10: 115,259,290 (GRCm39) |
Y1621H |
probably benign |
Het |
Zfp251 |
T |
C |
15: 76,738,607 (GRCm39) |
D162G |
possibly damaging |
Het |
Zfp292 |
T |
C |
4: 34,807,078 (GRCm39) |
T1994A |
probably benign |
Het |
Zfp791 |
A |
G |
8: 85,837,559 (GRCm39) |
Y102H |
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 |
|
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 |
|
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 |
|