Other mutations in this stock |
Total: 129 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
C |
A |
5: 114,371,397 (GRCm39) |
P1842Q |
probably damaging |
Het |
Aco2 |
G |
A |
15: 81,773,635 (GRCm39) |
R58Q |
probably null |
Het |
Acvr1 |
T |
C |
2: 58,338,385 (GRCm39) |
K446E |
probably damaging |
Het |
Adam39 |
T |
C |
8: 41,277,755 (GRCm39) |
Y49H |
probably benign |
Het |
Afg3l2 |
C |
T |
18: 67,554,365 (GRCm39) |
V446M |
probably damaging |
Het |
Aire |
A |
G |
10: 77,871,579 (GRCm39) |
V397A |
probably benign |
Het |
Ankdd1a |
C |
T |
9: 65,411,452 (GRCm39) |
A352T |
possibly damaging |
Het |
Aoc1l2 |
T |
C |
6: 48,907,909 (GRCm39) |
M303T |
probably benign |
Het |
Arfip2 |
T |
C |
7: 105,286,079 (GRCm39) |
D270G |
possibly damaging |
Het |
Arl4c |
A |
G |
1: 88,629,134 (GRCm39) |
C85R |
probably damaging |
Het |
Arpp21 |
A |
C |
9: 111,956,354 (GRCm39) |
V541G |
possibly damaging |
Het |
Atp2a3 |
T |
A |
11: 72,873,578 (GRCm39) |
M817K |
probably damaging |
Het |
Bahcc1 |
C |
T |
11: 120,150,035 (GRCm39) |
H106Y |
possibly damaging |
Het |
Bcl9l |
A |
G |
9: 44,412,076 (GRCm39) |
S21G |
possibly damaging |
Het |
C7 |
T |
A |
15: 5,086,579 (GRCm39) |
|
probably null |
Het |
Cabcoco1 |
T |
C |
10: 68,272,725 (GRCm39) |
D220G |
possibly damaging |
Het |
Cacna1e |
T |
A |
1: 154,283,486 (GRCm39) |
D1960V |
probably benign |
Het |
Casp4 |
A |
T |
9: 5,324,832 (GRCm39) |
T215S |
probably damaging |
Het |
Ccdc187 |
T |
C |
2: 26,183,698 (GRCm39) |
S101G |
possibly damaging |
Het |
Cdk12 |
A |
G |
11: 98,140,628 (GRCm39) |
N1290D |
unknown |
Het |
Cdo1 |
C |
A |
18: 46,861,104 (GRCm39) |
V36L |
probably benign |
Het |
Col5a3 |
G |
A |
9: 20,714,429 (GRCm39) |
A381V |
unknown |
Het |
Cspg4b |
T |
C |
13: 113,504,574 (GRCm39) |
I1901T |
|
Het |
Dcpp2 |
A |
G |
17: 24,119,453 (GRCm39) |
E89G |
probably damaging |
Het |
Dhx57 |
G |
T |
17: 80,561,817 (GRCm39) |
A899E |
probably damaging |
Het |
Dnaaf1 |
T |
C |
8: 120,309,392 (GRCm39) |
I160T |
probably damaging |
Het |
Dnah1 |
C |
A |
14: 30,986,394 (GRCm39) |
A3698S |
probably damaging |
Het |
Dnah12 |
C |
A |
14: 26,597,281 (GRCm39) |
R3547S |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,610,114 (GRCm39) |
V1774A |
probably benign |
Het |
Dop1a |
G |
A |
9: 86,424,811 (GRCm39) |
R2085Q |
probably damaging |
Het |
Duox1 |
T |
C |
2: 122,151,203 (GRCm39) |
Y293H |
probably damaging |
Het |
Efcab5 |
G |
A |
11: 77,022,934 (GRCm39) |
T593I |
probably damaging |
Het |
Elp1 |
G |
T |
4: 56,772,521 (GRCm39) |
P867T |
probably benign |
Het |
Epas1 |
T |
A |
17: 87,112,667 (GRCm39) |
D88E |
probably damaging |
Het |
Epdr1 |
A |
G |
13: 19,778,821 (GRCm39) |
F92L |
possibly damaging |
Het |
Ercc6 |
T |
C |
14: 32,296,924 (GRCm39) |
W1305R |
probably damaging |
Het |
Etv6 |
A |
G |
6: 134,225,672 (GRCm39) |
N212S |
probably benign |
Het |
Fam20b |
A |
T |
1: 156,530,010 (GRCm39) |
Y141* |
probably null |
Het |
Fancm |
A |
G |
12: 65,168,494 (GRCm39) |
N1619S |
probably damaging |
Het |
Fbln5 |
A |
T |
12: 101,734,722 (GRCm39) |
N183K |
probably damaging |
Het |
Fer1l6 |
A |
G |
15: 58,490,370 (GRCm39) |
D976G |
possibly damaging |
Het |
Fgb |
T |
C |
3: 82,952,409 (GRCm39) |
|
probably null |
Het |
Fhod1 |
A |
T |
8: 106,074,422 (GRCm39) |
Y22N |
unknown |
Het |
Foxl3 |
C |
A |
5: 138,807,213 (GRCm39) |
Q164K |
probably benign |
Het |
Galm |
C |
T |
17: 80,490,859 (GRCm39) |
Q166* |
probably null |
Het |
Gbe1 |
A |
T |
16: 70,198,664 (GRCm39) |
Y119F |
probably benign |
Het |
Gcnt7 |
T |
A |
2: 172,293,180 (GRCm39) |
Y369F |
probably damaging |
Het |
Gdap2 |
T |
C |
3: 100,099,006 (GRCm39) |
I366T |
possibly damaging |
Het |
Gm14295 |
T |
C |
2: 176,499,162 (GRCm39) |
V4A |
probably benign |
Het |
Gm32742 |
T |
A |
9: 51,068,327 (GRCm39) |
Y249F |
probably benign |
Het |
Gm40460 |
A |
T |
7: 141,794,701 (GRCm39) |
C39S |
unknown |
Het |
Gm6370 |
T |
A |
5: 146,429,281 (GRCm39) |
C120* |
probably null |
Het |
Harbi1 |
T |
A |
2: 91,542,698 (GRCm39) |
L53* |
probably null |
Het |
Herc3 |
A |
G |
6: 58,835,999 (GRCm39) |
N280S |
probably null |
Het |
Hipk2 |
T |
A |
6: 38,724,390 (GRCm39) |
R447W |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,312,786 (GRCm39) |
I4176V |
probably benign |
Het |
Ifi211 |
A |
T |
1: 173,733,052 (GRCm39) |
I203N |
probably benign |
Het |
Kcnc1 |
G |
A |
7: 46,077,010 (GRCm39) |
V271M |
probably benign |
Het |
Kcng1 |
T |
A |
2: 168,104,797 (GRCm39) |
I350F |
probably damaging |
Het |
Kif21b |
A |
T |
1: 136,077,090 (GRCm39) |
I371F |
probably damaging |
Het |
Klrc1 |
A |
G |
6: 129,655,746 (GRCm39) |
F43S |
probably damaging |
Het |
Krtap6-2 |
A |
G |
16: 89,216,722 (GRCm39) |
S82P |
unknown |
Het |
Lamb1 |
T |
A |
12: 31,322,492 (GRCm39) |
M186K |
probably damaging |
Het |
Lrig2 |
T |
C |
3: 104,375,924 (GRCm39) |
K451E |
possibly damaging |
Het |
Lrrc15 |
G |
A |
16: 30,093,016 (GRCm39) |
L108F |
probably damaging |
Het |
Mark3 |
A |
G |
12: 111,570,960 (GRCm39) |
I87V |
probably damaging |
Het |
Mlh1 |
T |
C |
9: 111,060,013 (GRCm39) |
K622E |
|
Het |
Mrgprb2 |
G |
A |
7: 48,202,674 (GRCm39) |
T17M |
possibly damaging |
Het |
Msantd5f4 |
G |
T |
4: 73,557,190 (GRCm39) |
V8F |
probably damaging |
Het |
Mtmr4 |
C |
T |
11: 87,493,241 (GRCm39) |
R225C |
probably damaging |
Het |
Nfatc1 |
A |
G |
18: 80,678,916 (GRCm39) |
L824P |
probably damaging |
Het |
Nlrp4f |
A |
T |
13: 65,347,053 (GRCm39) |
D46E |
probably damaging |
Het |
Oga |
CTCGGGTC |
CTC |
19: 45,743,096 (GRCm39) |
|
probably null |
Het |
Or10h5 |
G |
T |
17: 33,434,415 (GRCm39) |
T301N |
probably benign |
Het |
Or13n4 |
A |
C |
7: 106,423,020 (GRCm39) |
F238V |
probably damaging |
Het |
Or1l4 |
G |
T |
2: 37,091,575 (GRCm39) |
M107I |
probably benign |
Het |
Or2w25 |
T |
A |
11: 59,504,580 (GRCm39) |
N263K |
probably damaging |
Het |
Or6z7 |
G |
C |
7: 6,483,243 (GRCm39) |
A304G |
probably null |
Het |
Or7e173 |
T |
A |
9: 19,939,045 (GRCm39) |
Y63F |
probably damaging |
Het |
Or8b1 |
G |
T |
9: 38,400,092 (GRCm39) |
A256S |
possibly damaging |
Het |
Otulin |
A |
G |
15: 27,608,812 (GRCm39) |
Y244H |
probably damaging |
Het |
Pabpc4 |
T |
C |
4: 123,180,653 (GRCm39) |
I125T |
probably damaging |
Het |
Parp14 |
A |
G |
16: 35,677,775 (GRCm39) |
I731T |
probably benign |
Het |
Parp8 |
T |
C |
13: 117,029,631 (GRCm39) |
T531A |
probably benign |
Het |
Parvg |
G |
T |
15: 84,213,065 (GRCm39) |
V49L |
probably benign |
Het |
Pcdha12 |
T |
C |
18: 37,155,284 (GRCm39) |
S668P |
probably damaging |
Het |
Pcdhb9 |
A |
C |
18: 37,534,665 (GRCm39) |
N220H |
probably benign |
Het |
Pcdhga4 |
T |
G |
18: 37,819,527 (GRCm39) |
S359A |
probably benign |
Het |
Pi4k2b |
T |
A |
5: 52,908,799 (GRCm39) |
S208R |
probably damaging |
Het |
Pm20d1 |
G |
A |
1: 131,730,501 (GRCm39) |
V252I |
probably damaging |
Het |
Pxdc1 |
T |
A |
13: 34,836,258 (GRCm39) |
H54L |
probably damaging |
Het |
Rag1 |
A |
T |
2: 101,473,327 (GRCm39) |
V605E |
probably damaging |
Het |
Rasgrf2 |
A |
T |
13: 92,034,469 (GRCm39) |
|
probably null |
Het |
Relch |
T |
C |
1: 105,591,876 (GRCm39) |
V15A |
probably damaging |
Het |
Rflnb |
T |
A |
11: 75,912,951 (GRCm39) |
T146S |
probably damaging |
Het |
Rfx5 |
T |
A |
3: 94,866,639 (GRCm39) |
L646Q |
unknown |
Het |
Rnf43 |
A |
G |
11: 87,618,891 (GRCm39) |
T81A |
probably benign |
Het |
Ros1 |
T |
C |
10: 51,943,170 (GRCm39) |
D2048G |
probably damaging |
Het |
Rpl13a-ps1 |
T |
A |
19: 50,018,612 (GRCm39) |
K188I |
possibly damaging |
Het |
Rpl24 |
T |
A |
16: 55,790,509 (GRCm39) |
S122T |
probably benign |
Het |
Ryr2 |
G |
A |
13: 11,760,104 (GRCm39) |
T1549M |
probably damaging |
Het |
Sbf2 |
T |
C |
7: 110,040,702 (GRCm39) |
Q375R |
possibly damaging |
Het |
Sec23a |
A |
T |
12: 59,048,817 (GRCm39) |
F131I |
possibly damaging |
Het |
Secisbp2 |
T |
C |
13: 51,837,320 (GRCm39) |
I827T |
probably damaging |
Het |
Serpinb6d |
A |
G |
13: 33,854,756 (GRCm39) |
R244G |
probably benign |
Het |
Skor2 |
C |
T |
18: 76,946,376 (GRCm39) |
H33Y |
unknown |
Het |
Snx17 |
C |
A |
5: 31,355,088 (GRCm39) |
Q368K |
probably damaging |
Het |
Stac |
T |
A |
9: 111,401,411 (GRCm39) |
E345V |
probably benign |
Het |
Stx4a |
A |
G |
7: 127,445,375 (GRCm39) |
N164S |
possibly damaging |
Het |
Tasor |
T |
C |
14: 27,201,766 (GRCm39) |
|
probably null |
Het |
Tbcb |
A |
T |
7: 29,930,549 (GRCm39) |
|
probably null |
Het |
Tecpr2 |
T |
C |
12: 110,914,141 (GRCm39) |
S1151P |
possibly damaging |
Het |
Timm50 |
A |
G |
7: 28,007,069 (GRCm39) |
F202S |
possibly damaging |
Het |
Tle2 |
A |
G |
10: 81,417,567 (GRCm39) |
D244G |
probably benign |
Het |
Tlr4 |
G |
A |
4: 66,759,522 (GRCm39) |
V772I |
possibly damaging |
Het |
Tmem214 |
G |
A |
5: 31,027,043 (GRCm39) |
W11* |
probably null |
Het |
Tmem241 |
A |
T |
18: 12,176,356 (GRCm39) |
L227* |
probably null |
Het |
Top2b |
A |
C |
14: 16,365,718 (GRCm38) |
T14P |
probably benign |
Het |
Trim44 |
T |
C |
2: 102,187,827 (GRCm39) |
T309A |
probably benign |
Het |
Trps1 |
A |
C |
15: 50,524,657 (GRCm39) |
I1091S |
probably damaging |
Het |
Tspan2 |
C |
A |
3: 102,672,583 (GRCm39) |
T200K |
probably damaging |
Het |
Tuba8 |
A |
G |
6: 121,200,063 (GRCm39) |
N249S |
probably benign |
Het |
Vmn1r189 |
A |
G |
13: 22,286,426 (GRCm39) |
L137P |
probably damaging |
Het |
Vmn2r29 |
A |
T |
7: 7,244,855 (GRCm39) |
W340R |
probably benign |
Het |
Vmn2r52 |
A |
C |
7: 9,893,476 (GRCm39) |
D554E |
probably benign |
Het |
Zc3h4 |
C |
G |
7: 16,168,891 (GRCm39) |
P1075R |
unknown |
Het |
Zfp599 |
A |
G |
9: 22,160,999 (GRCm39) |
S389P |
probably damaging |
Het |
Zfp777 |
A |
T |
6: 48,021,580 (GRCm39) |
V14D |
possibly damaging |
Het |
Zswim8 |
C |
T |
14: 20,762,150 (GRCm39) |
Q262* |
probably null |
Het |
|
Other mutations in Plxnb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00546:Plxnb2
|
APN |
15 |
89,046,569 (GRCm39) |
splice site |
probably benign |
|
IGL01574:Plxnb2
|
APN |
15 |
89,046,886 (GRCm39) |
splice site |
probably null |
|
IGL01695:Plxnb2
|
APN |
15 |
89,041,417 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01763:Plxnb2
|
APN |
15 |
89,046,184 (GRCm39) |
splice site |
probably null |
|
IGL01921:Plxnb2
|
APN |
15 |
89,048,474 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02129:Plxnb2
|
APN |
15 |
89,044,613 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02153:Plxnb2
|
APN |
15 |
89,050,016 (GRCm39) |
nonsense |
probably null |
|
IGL02637:Plxnb2
|
APN |
15 |
89,048,260 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02892:Plxnb2
|
APN |
15 |
89,045,425 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03108:Plxnb2
|
APN |
15 |
89,042,234 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03115:Plxnb2
|
APN |
15 |
89,046,641 (GRCm39) |
splice site |
probably benign |
|
P0040:Plxnb2
|
UTSW |
15 |
89,047,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Plxnb2
|
UTSW |
15 |
89,047,479 (GRCm39) |
critical splice donor site |
probably null |
|
R0095:Plxnb2
|
UTSW |
15 |
89,049,534 (GRCm39) |
missense |
probably benign |
|
R0103:Plxnb2
|
UTSW |
15 |
89,045,972 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0544:Plxnb2
|
UTSW |
15 |
89,042,816 (GRCm39) |
splice site |
probably benign |
|
R0671:Plxnb2
|
UTSW |
15 |
89,042,184 (GRCm39) |
missense |
probably benign |
0.14 |
R1279:Plxnb2
|
UTSW |
15 |
89,046,524 (GRCm39) |
missense |
probably benign |
0.02 |
R1530:Plxnb2
|
UTSW |
15 |
89,051,395 (GRCm39) |
missense |
probably benign |
|
R1542:Plxnb2
|
UTSW |
15 |
89,050,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R1610:Plxnb2
|
UTSW |
15 |
89,042,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1686:Plxnb2
|
UTSW |
15 |
89,046,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Plxnb2
|
UTSW |
15 |
89,046,187 (GRCm39) |
critical splice donor site |
probably null |
|
R1996:Plxnb2
|
UTSW |
15 |
89,042,971 (GRCm39) |
missense |
probably benign |
0.13 |
R1997:Plxnb2
|
UTSW |
15 |
89,042,971 (GRCm39) |
missense |
probably benign |
0.13 |
R2031:Plxnb2
|
UTSW |
15 |
89,047,013 (GRCm39) |
nonsense |
probably null |
|
R2049:Plxnb2
|
UTSW |
15 |
89,043,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Plxnb2
|
UTSW |
15 |
89,042,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2076:Plxnb2
|
UTSW |
15 |
89,042,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Plxnb2
|
UTSW |
15 |
89,040,765 (GRCm39) |
missense |
probably benign |
0.04 |
R2418:Plxnb2
|
UTSW |
15 |
89,045,272 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2419:Plxnb2
|
UTSW |
15 |
89,045,272 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3752:Plxnb2
|
UTSW |
15 |
89,041,458 (GRCm39) |
splice site |
probably benign |
|
R3825:Plxnb2
|
UTSW |
15 |
89,050,602 (GRCm39) |
missense |
probably benign |
0.05 |
R4154:Plxnb2
|
UTSW |
15 |
89,043,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R4197:Plxnb2
|
UTSW |
15 |
89,041,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Plxnb2
|
UTSW |
15 |
89,044,826 (GRCm39) |
missense |
probably damaging |
0.96 |
R4434:Plxnb2
|
UTSW |
15 |
89,047,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Plxnb2
|
UTSW |
15 |
89,045,131 (GRCm39) |
missense |
probably benign |
0.37 |
R4717:Plxnb2
|
UTSW |
15 |
89,041,622 (GRCm39) |
nonsense |
probably null |
|
R4773:Plxnb2
|
UTSW |
15 |
89,051,150 (GRCm39) |
missense |
probably benign |
0.06 |
R4905:Plxnb2
|
UTSW |
15 |
89,041,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R5368:Plxnb2
|
UTSW |
15 |
89,043,796 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5418:Plxnb2
|
UTSW |
15 |
89,050,694 (GRCm39) |
missense |
probably benign |
0.00 |
R5484:Plxnb2
|
UTSW |
15 |
89,048,412 (GRCm39) |
splice site |
probably null |
|
R5520:Plxnb2
|
UTSW |
15 |
89,051,746 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5566:Plxnb2
|
UTSW |
15 |
89,048,223 (GRCm39) |
missense |
probably benign |
0.05 |
R5568:Plxnb2
|
UTSW |
15 |
89,041,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5619:Plxnb2
|
UTSW |
15 |
89,047,012 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5685:Plxnb2
|
UTSW |
15 |
89,051,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R5688:Plxnb2
|
UTSW |
15 |
89,042,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5809:Plxnb2
|
UTSW |
15 |
89,051,774 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5813:Plxnb2
|
UTSW |
15 |
89,044,962 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5866:Plxnb2
|
UTSW |
15 |
89,051,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R6016:Plxnb2
|
UTSW |
15 |
89,045,225 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6117:Plxnb2
|
UTSW |
15 |
89,042,203 (GRCm39) |
missense |
probably benign |
0.04 |
R6187:Plxnb2
|
UTSW |
15 |
89,051,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Plxnb2
|
UTSW |
15 |
89,049,494 (GRCm39) |
missense |
probably benign |
0.22 |
R6263:Plxnb2
|
UTSW |
15 |
89,046,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R6269:Plxnb2
|
UTSW |
15 |
89,044,916 (GRCm39) |
missense |
probably benign |
0.18 |
R6351:Plxnb2
|
UTSW |
15 |
89,041,973 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6522:Plxnb2
|
UTSW |
15 |
89,048,629 (GRCm39) |
missense |
probably benign |
0.18 |
R6856:Plxnb2
|
UTSW |
15 |
89,048,523 (GRCm39) |
missense |
probably benign |
0.27 |
R6930:Plxnb2
|
UTSW |
15 |
89,044,592 (GRCm39) |
missense |
probably benign |
|
R7354:Plxnb2
|
UTSW |
15 |
89,049,928 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7513:Plxnb2
|
UTSW |
15 |
89,042,525 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7522:Plxnb2
|
UTSW |
15 |
89,045,977 (GRCm39) |
missense |
probably benign |
0.20 |
R7730:Plxnb2
|
UTSW |
15 |
89,046,533 (GRCm39) |
missense |
probably benign |
|
R7766:Plxnb2
|
UTSW |
15 |
89,045,474 (GRCm39) |
missense |
probably benign |
0.01 |
R7781:Plxnb2
|
UTSW |
15 |
89,041,225 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8126:Plxnb2
|
UTSW |
15 |
89,047,506 (GRCm39) |
missense |
probably benign |
|
R8131:Plxnb2
|
UTSW |
15 |
89,042,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R8372:Plxnb2
|
UTSW |
15 |
89,042,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8736:Plxnb2
|
UTSW |
15 |
89,046,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8772:Plxnb2
|
UTSW |
15 |
89,046,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R9022:Plxnb2
|
UTSW |
15 |
89,048,471 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9044:Plxnb2
|
UTSW |
15 |
89,044,566 (GRCm39) |
splice site |
probably benign |
|
R9253:Plxnb2
|
UTSW |
15 |
89,052,015 (GRCm39) |
missense |
probably benign |
|
R9398:Plxnb2
|
UTSW |
15 |
89,045,122 (GRCm39) |
missense |
probably benign |
0.02 |
R9568:Plxnb2
|
UTSW |
15 |
89,045,160 (GRCm39) |
nonsense |
probably null |
|
R9613:Plxnb2
|
UTSW |
15 |
89,048,496 (GRCm39) |
missense |
probably benign |
0.01 |
X0027:Plxnb2
|
UTSW |
15 |
89,044,916 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Plxnb2
|
UTSW |
15 |
89,043,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|