Other mutations in this stock |
Total: 137 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
C |
A |
15: 64,694,162 (GRCm39) |
V372L |
probably benign |
Het |
Bod1l |
T |
C |
5: 41,986,208 (GRCm39) |
D458G |
probably benign |
Het |
Cacna1c |
G |
T |
6: 118,590,256 (GRCm39) |
H1416N |
probably damaging |
Het |
Cacna2d1 |
T |
C |
5: 16,140,067 (GRCm39) |
I19T |
probably benign |
Het |
Cadps |
T |
A |
14: 12,715,374 (GRCm38) |
T153S |
possibly damaging |
Het |
Cd200r1 |
A |
T |
16: 44,614,672 (GRCm39) |
D317V |
possibly damaging |
Het |
Cimap1c |
T |
C |
9: 56,756,341 (GRCm39) |
E225G |
probably benign |
Het |
Dcaf5 |
C |
T |
12: 80,385,606 (GRCm39) |
R840H |
probably benign |
Het |
Dnhd1 |
A |
C |
7: 105,370,895 (GRCm39) |
H4725P |
possibly damaging |
Het |
Echdc3 |
C |
A |
2: 6,200,538 (GRCm39) |
L149F |
probably benign |
Het |
Efhb |
T |
G |
17: 53,769,649 (GRCm39) |
Q220P |
possibly damaging |
Het |
Efr3b |
A |
T |
12: 4,025,411 (GRCm39) |
Y18* |
probably null |
Het |
Eri1 |
T |
C |
8: 35,949,836 (GRCm39) |
K41R |
possibly damaging |
Het |
Eri1 |
C |
A |
8: 35,949,800 (GRCm39) |
G53V |
probably benign |
Het |
Gm10212 |
A |
G |
19: 11,546,924 (GRCm39) |
|
noncoding transcript |
Het |
Gm11168 |
T |
G |
9: 3,005,124 (GRCm39) |
F201C |
probably damaging |
Het |
Gm14412 |
A |
C |
2: 177,007,479 (GRCm39) |
S139A |
probably benign |
Het |
Gm21411 |
C |
T |
4: 146,977,067 (GRCm39) |
S69N |
possibly damaging |
Het |
Gm21738 |
A |
G |
14: 19,418,885 (GRCm38) |
C16R |
probably benign |
Het |
Gm21967 |
T |
A |
13: 120,071,071 (GRCm39) |
|
probably benign |
Het |
Gm4952 |
A |
T |
19: 12,600,987 (GRCm39) |
D69V |
probably damaging |
Het |
Gm5591 |
T |
G |
7: 38,219,838 (GRCm39) |
K345T |
probably benign |
Het |
Gm7647 |
T |
C |
5: 95,110,839 (GRCm39) |
S7P |
probably benign |
Het |
Gm9758 |
G |
A |
5: 14,963,522 (GRCm39) |
|
probably benign |
Het |
Gtse1 |
C |
A |
15: 85,753,018 (GRCm39) |
Q378K |
possibly damaging |
Het |
Haus3 |
T |
C |
5: 34,323,690 (GRCm39) |
K307E |
probably benign |
Het |
Hjurp |
A |
G |
1: 88,197,991 (GRCm39) |
L96S |
probably benign |
Het |
Ifi205 |
T |
A |
1: 173,854,899 (GRCm39) |
|
probably benign |
Het |
Ighg1 |
A |
G |
12: 113,292,804 (GRCm39) |
V255A |
unknown |
Het |
Ighv14-4 |
T |
A |
12: 114,140,252 (GRCm39) |
M49L |
probably benign |
Het |
Jak1 |
A |
C |
4: 101,028,554 (GRCm39) |
L508R |
probably damaging |
Het |
Kif18a |
A |
G |
2: 109,164,767 (GRCm39) |
Q821R |
probably benign |
Het |
Kif21b |
T |
C |
1: 136,080,080 (GRCm39) |
S539P |
possibly damaging |
Het |
Klhdc2 |
T |
C |
12: 69,353,987 (GRCm39) |
V266A |
probably benign |
Het |
Lonp2 |
G |
T |
8: 87,368,161 (GRCm39) |
|
probably benign |
Het |
Mpdz |
C |
T |
4: 81,221,821 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
G |
T |
1: 88,172,692 (GRCm39) |
M823I |
probably benign |
Het |
Mroh2a |
G |
A |
1: 88,161,842 (GRCm39) |
G309D |
possibly damaging |
Het |
Mroh2a |
G |
A |
1: 88,158,468 (GRCm39) |
E172K |
probably damaging |
Het |
Mtif3 |
C |
A |
5: 146,895,914 (GRCm39) |
G58* |
probably null |
Het |
Muc4 |
C |
T |
16: 32,576,179 (GRCm39) |
|
probably benign |
Het |
Muc4 |
C |
T |
16: 32,575,114 (GRCm39) |
P1233L |
probably benign |
Het |
Muc4 |
G |
T |
16: 32,575,139 (GRCm39) |
K1241N |
probably benign |
Het |
Muc4 |
G |
A |
16: 32,575,140 (GRCm39) |
G1242R |
probably benign |
Het |
Muc4 |
T |
G |
16: 32,753,863 (GRCm38) |
N1246K |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,753,886 (GRCm38) |
E1254V |
probably benign |
Het |
Muc4 |
C |
T |
16: 32,752,569 (GRCm38) |
P816S |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,575,362 (GRCm39) |
R1316G |
probably benign |
Het |
Muc4 |
C |
A |
16: 32,575,246 (GRCm39) |
T1277K |
possibly damaging |
Het |
Muc6 |
C |
T |
7: 141,638,890 (GRCm38) |
A1957T |
possibly damaging |
Het |
Naca |
T |
A |
10: 127,879,669 (GRCm39) |
|
probably benign |
Het |
Nars2 |
A |
T |
7: 96,651,997 (GRCm39) |
|
probably benign |
Het |
Or1j14 |
A |
C |
2: 36,418,005 (GRCm39) |
I194L |
probably benign |
Het |
Or52b3 |
G |
T |
7: 102,204,098 (GRCm39) |
L202F |
probably damaging |
Het |
Or5b12b |
G |
T |
19: 12,861,265 (GRCm39) |
V7L |
probably benign |
Het |
Or6c216 |
T |
C |
10: 129,678,342 (GRCm39) |
T190A |
probably damaging |
Het |
Pcdh7 |
G |
A |
5: 57,877,806 (GRCm39) |
E454K |
possibly damaging |
Het |
Pip5kl1 |
C |
A |
2: 32,473,359 (GRCm39) |
A332D |
probably benign |
Het |
Pisd |
A |
T |
5: 32,896,702 (GRCm39) |
S280T |
probably benign |
Het |
Pramel34 |
T |
A |
5: 93,784,336 (GRCm39) |
Q376L |
probably damaging |
Het |
Pramel5 |
A |
G |
4: 144,000,549 (GRCm39) |
L9P |
probably damaging |
Het |
Prkd3 |
G |
T |
17: 79,261,952 (GRCm39) |
N787K |
probably benign |
Het |
Prkdc |
A |
T |
16: 15,519,979 (GRCm39) |
H1139L |
probably benign |
Het |
R3hdm1 |
A |
G |
1: 128,089,933 (GRCm39) |
|
probably benign |
Het |
Rbfox2 |
T |
C |
15: 76,987,136 (GRCm39) |
N206D |
probably damaging |
Het |
Rlf |
T |
C |
4: 121,005,536 (GRCm39) |
E1258G |
possibly damaging |
Het |
Rpl8 |
T |
C |
15: 76,789,242 (GRCm39) |
|
probably benign |
Het |
Senp5 |
A |
C |
16: 31,809,092 (GRCm39) |
V27G |
probably benign |
Het |
Serpina1b |
T |
A |
12: 103,694,525 (GRCm39) |
K406N |
probably damaging |
Het |
Sfi1 |
G |
A |
11: 3,084,337 (GRCm39) |
A975V |
probably benign |
Het |
Sfi1 |
T |
C |
11: 3,093,689 (GRCm39) |
|
probably benign |
Het |
Sfi1 |
C |
T |
11: 3,085,671 (GRCm39) |
A853T |
probably damaging |
Het |
Shc1 |
T |
C |
3: 89,331,536 (GRCm39) |
S154P |
probably damaging |
Het |
Sirpd |
C |
T |
3: 15,397,205 (GRCm39) |
|
probably null |
Het |
Skint5 |
A |
G |
4: 113,400,070 (GRCm39) |
|
probably null |
Het |
Slc17a8 |
T |
C |
10: 89,412,392 (GRCm39) |
D531G |
probably benign |
Het |
Slc4a10 |
A |
C |
2: 62,117,284 (GRCm39) |
T718P |
probably damaging |
Het |
Slc7a11 |
C |
T |
3: 50,333,518 (GRCm39) |
R411Q |
probably damaging |
Het |
Slitrk3 |
A |
G |
3: 72,957,414 (GRCm39) |
F453L |
probably damaging |
Het |
Slk |
A |
C |
19: 47,568,691 (GRCm39) |
Q20P |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,250,345 (GRCm39) |
|
probably null |
Het |
Sp110 |
G |
A |
1: 85,514,002 (GRCm39) |
R252C |
possibly damaging |
Het |
Sp140 |
C |
T |
1: 85,553,886 (GRCm39) |
R242C |
possibly damaging |
Het |
Sp140 |
G |
A |
1: 85,553,854 (GRCm39) |
R231K |
probably benign |
Het |
Speer4a3 |
A |
C |
5: 26,159,222 (GRCm39) |
W41G |
probably benign |
Het |
Speer4b |
G |
A |
5: 27,706,272 (GRCm39) |
P30S |
probably damaging |
Het |
Spef1l |
A |
C |
7: 139,558,016 (GRCm39) |
V60G |
probably damaging |
Het |
Stim1 |
T |
A |
7: 102,075,954 (GRCm39) |
H395Q |
probably damaging |
Het |
Sult2a1 |
T |
C |
7: 13,537,961 (GRCm39) |
I187M |
probably benign |
Het |
Thap1 |
G |
A |
8: 26,652,759 (GRCm39) |
D189N |
probably benign |
Het |
Thap1 |
C |
T |
8: 26,650,910 (GRCm39) |
P37L |
possibly damaging |
Het |
Thrap3 |
C |
T |
4: 126,059,188 (GRCm39) |
|
probably benign |
Het |
Tmem132d |
C |
T |
5: 127,861,896 (GRCm39) |
V742I |
possibly damaging |
Het |
Tmprss9 |
A |
G |
10: 80,728,126 (GRCm39) |
D572G |
possibly damaging |
Het |
Tmtc1 |
T |
G |
6: 148,345,442 (GRCm39) |
T86P |
probably benign |
Het |
Trip12 |
A |
T |
1: 84,729,605 (GRCm39) |
N1026K |
probably damaging |
Het |
Ttll5 |
T |
A |
12: 85,923,363 (GRCm39) |
V280E |
probably damaging |
Het |
Ubn2 |
T |
A |
6: 38,459,540 (GRCm39) |
D592E |
possibly damaging |
Het |
Ubr1 |
T |
G |
2: 120,761,353 (GRCm39) |
H608P |
probably damaging |
Het |
Ugt1a6b |
A |
T |
1: 88,142,900 (GRCm39) |
|
probably null |
Het |
Vmn1r77 |
C |
A |
7: 11,775,695 (GRCm39) |
S89Y |
probably benign |
Het |
Vmn1r77 |
A |
C |
7: 11,775,403 (GRCm39) |
I60L |
probably benign |
Het |
Vmn2r114 |
G |
A |
17: 23,509,939 (GRCm39) |
A847V |
probably benign |
Het |
Vmn2r114 |
A |
T |
17: 23,510,212 (GRCm39) |
L756Q |
probably damaging |
Het |
Vmn2r114 |
G |
T |
17: 23,509,957 (GRCm39) |
S841Y |
probably benign |
Het |
Vmn2r116 |
C |
T |
17: 23,606,210 (GRCm39) |
S374F |
probably benign |
Het |
Vmn2r116 |
C |
T |
17: 23,616,701 (GRCm39) |
P540S |
probably damaging |
Het |
Vmn2r117 |
T |
G |
17: 23,694,403 (GRCm39) |
K481N |
probably damaging |
Het |
Vmn2r117 |
C |
T |
17: 23,696,814 (GRCm39) |
A198T |
probably damaging |
Het |
Vmn2r117 |
A |
C |
17: 23,698,520 (GRCm39) |
S18A |
probably benign |
Het |
Vmn2r121 |
T |
A |
X: 123,037,480 (GRCm39) |
N847Y |
possibly damaging |
Het |
Vmn2r121 |
C |
T |
X: 123,043,413 (GRCm39) |
E73K |
probably benign |
Het |
Vmn2r121 |
T |
G |
X: 123,037,499 (GRCm39) |
K840N |
probably benign |
Het |
Vmn2r125 |
T |
C |
4: 156,703,678 (GRCm39) |
M352T |
probably benign |
Het |
Vmn2r125 |
T |
A |
4: 156,703,521 (GRCm39) |
L300M |
probably benign |
Het |
Vmn2r125 |
A |
T |
4: 156,703,332 (GRCm39) |
T237S |
probably benign |
Het |
Vmn2r125 |
C |
T |
4: 156,703,333 (GRCm39) |
T237I |
probably benign |
Het |
Vmn2r125 |
C |
A |
4: 156,703,194 (GRCm39) |
Q191K |
probably benign |
Het |
Vmn2r125 |
A |
C |
4: 156,703,195 (GRCm39) |
Q191P |
probably benign |
Het |
Vmn2r125 |
T |
C |
4: 156,703,261 (GRCm39) |
V213A |
probably benign |
Het |
Vmn2r129 |
C |
A |
4: 156,690,730 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r129 |
A |
T |
4: 156,690,441 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r129 |
T |
G |
4: 156,690,779 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r129 |
T |
G |
4: 156,686,857 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r129 |
T |
C |
4: 156,686,558 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r129 |
G |
T |
4: 156,690,755 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r88 |
A |
G |
14: 51,650,582 (GRCm39) |
I98M |
probably benign |
Het |
Vmn2r88 |
C |
T |
14: 51,654,259 (GRCm39) |
P539L |
possibly damaging |
Het |
Vmn2r88 |
T |
C |
14: 51,650,713 (GRCm39) |
I142T |
probably benign |
Het |
Vmn2r88 |
T |
C |
14: 51,650,517 (GRCm39) |
F77L |
probably benign |
Het |
Vmn2r89 |
A |
C |
14: 51,693,428 (GRCm39) |
Q259H |
probably benign |
Het |
Vmn2r89 |
T |
G |
14: 51,694,950 (GRCm39) |
L477V |
probably benign |
Het |
Zfp180 |
C |
T |
7: 23,804,255 (GRCm39) |
R225C |
probably benign |
Het |
Zfp180 |
G |
A |
7: 23,803,841 (GRCm39) |
C85Y |
possibly damaging |
Het |
Zfp180 |
G |
A |
7: 23,804,420 (GRCm39) |
V280M |
possibly damaging |
Het |
Zfp982 |
G |
A |
4: 147,596,826 (GRCm39) |
C61Y |
probably benign |
Het |
|
Other mutations in Vmn2r115 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Vmn2r115
|
APN |
17 |
23,575,934 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00990:Vmn2r115
|
APN |
17 |
23,565,346 (GRCm39) |
missense |
probably benign |
0.30 |
IGL00990:Vmn2r115
|
APN |
17 |
23,565,345 (GRCm39) |
nonsense |
probably null |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,565,135 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00990:Vmn2r115
|
APN |
17 |
23,565,252 (GRCm39) |
missense |
probably benign |
0.14 |
IGL00990:Vmn2r115
|
APN |
17 |
23,565,313 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Vmn2r115
|
APN |
17 |
23,578,323 (GRCm39) |
missense |
probably benign |
0.22 |
IGL00990:Vmn2r115
|
APN |
17 |
23,565,150 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00990:Vmn2r115
|
APN |
17 |
23,565,180 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL00990:Vmn2r115
|
APN |
17 |
23,567,008 (GRCm39) |
nonsense |
probably null |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,578,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Vmn2r115
|
APN |
17 |
23,578,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Vmn2r115
|
APN |
17 |
23,565,238 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01073:Vmn2r115
|
APN |
17 |
23,564,971 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01101:Vmn2r115
|
APN |
17 |
23,564,971 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01300:Vmn2r115
|
APN |
17 |
23,578,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01415:Vmn2r115
|
APN |
17 |
23,578,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02309:Vmn2r115
|
APN |
17 |
23,564,113 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02863:Vmn2r115
|
APN |
17 |
23,578,257 (GRCm39) |
missense |
probably damaging |
0.97 |
R0023:Vmn2r115
|
UTSW |
17 |
23,565,252 (GRCm39) |
missense |
probably benign |
0.14 |
R0197:Vmn2r115
|
UTSW |
17 |
23,578,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R0361:Vmn2r115
|
UTSW |
17 |
23,564,196 (GRCm39) |
missense |
probably benign |
0.11 |
R0601:Vmn2r115
|
UTSW |
17 |
23,579,074 (GRCm39) |
missense |
probably null |
0.51 |
R0676:Vmn2r115
|
UTSW |
17 |
23,565,238 (GRCm39) |
missense |
probably benign |
0.19 |
R0685:Vmn2r115
|
UTSW |
17 |
23,578,249 (GRCm39) |
missense |
probably benign |
|
R0865:Vmn2r115
|
UTSW |
17 |
23,565,382 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1124:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1145:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1146:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1207:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1266:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1318:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1367:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1376:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1376:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1420:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1469:Vmn2r115
|
UTSW |
17 |
23,564,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R1469:Vmn2r115
|
UTSW |
17 |
23,564,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R1604:Vmn2r115
|
UTSW |
17 |
23,564,245 (GRCm39) |
missense |
probably benign |
0.12 |
R1645:Vmn2r115
|
UTSW |
17 |
23,565,192 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1646:Vmn2r115
|
UTSW |
17 |
23,578,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1678:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1716:Vmn2r115
|
UTSW |
17 |
23,566,795 (GRCm39) |
missense |
probably benign |
|
R1846:Vmn2r115
|
UTSW |
17 |
23,578,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1885:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R1887:Vmn2r115
|
UTSW |
17 |
23,565,007 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1937:Vmn2r115
|
UTSW |
17 |
23,578,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R2007:Vmn2r115
|
UTSW |
17 |
23,566,927 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2120:Vmn2r115
|
UTSW |
17 |
23,578,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R3161:Vmn2r115
|
UTSW |
17 |
23,575,998 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3780:Vmn2r115
|
UTSW |
17 |
23,564,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R3982:Vmn2r115
|
UTSW |
17 |
23,578,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4019:Vmn2r115
|
UTSW |
17 |
23,579,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R4039:Vmn2r115
|
UTSW |
17 |
23,564,077 (GRCm39) |
missense |
probably benign |
0.26 |
R4087:Vmn2r115
|
UTSW |
17 |
23,565,358 (GRCm39) |
missense |
probably benign |
0.35 |
R4089:Vmn2r115
|
UTSW |
17 |
23,565,358 (GRCm39) |
missense |
probably benign |
0.35 |
R4379:Vmn2r115
|
UTSW |
17 |
23,564,197 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4417:Vmn2r115
|
UTSW |
17 |
23,564,854 (GRCm39) |
missense |
probably benign |
0.02 |
R4601:Vmn2r115
|
UTSW |
17 |
23,565,373 (GRCm39) |
missense |
probably benign |
0.01 |
R4874:Vmn2r115
|
UTSW |
17 |
23,578,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R5466:Vmn2r115
|
UTSW |
17 |
23,579,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R5613:Vmn2r115
|
UTSW |
17 |
23,564,307 (GRCm39) |
missense |
probably benign |
|
R5821:Vmn2r115
|
UTSW |
17 |
23,566,937 (GRCm39) |
missense |
probably damaging |
0.99 |
R6120:Vmn2r115
|
UTSW |
17 |
23,565,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R6193:Vmn2r115
|
UTSW |
17 |
23,575,983 (GRCm39) |
missense |
probably benign |
0.01 |
R6213:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R6290:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
R6319:Vmn2r115
|
UTSW |
17 |
23,566,877 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6495:Vmn2r115
|
UTSW |
17 |
23,578,572 (GRCm39) |
missense |
probably benign |
0.02 |
R6599:Vmn2r115
|
UTSW |
17 |
23,565,006 (GRCm39) |
missense |
probably benign |
0.00 |
R6764:Vmn2r115
|
UTSW |
17 |
23,565,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R6970:Vmn2r115
|
UTSW |
17 |
23,564,989 (GRCm39) |
missense |
probably benign |
0.23 |
R7023:Vmn2r115
|
UTSW |
17 |
23,578,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Vmn2r115
|
UTSW |
17 |
23,578,576 (GRCm39) |
missense |
probably benign |
0.01 |
R7353:Vmn2r115
|
UTSW |
17 |
23,564,887 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7483:Vmn2r115
|
UTSW |
17 |
23,565,371 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7743:Vmn2r115
|
UTSW |
17 |
23,564,772 (GRCm39) |
nonsense |
probably null |
|
R8005:Vmn2r115
|
UTSW |
17 |
23,563,124 (GRCm39) |
nonsense |
probably null |
|
R8191:Vmn2r115
|
UTSW |
17 |
23,578,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R8544:Vmn2r115
|
UTSW |
17 |
23,564,773 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8890:Vmn2r115
|
UTSW |
17 |
23,578,497 (GRCm39) |
missense |
probably damaging |
0.98 |
R9098:Vmn2r115
|
UTSW |
17 |
23,564,803 (GRCm39) |
missense |
probably benign |
|
R9114:Vmn2r115
|
UTSW |
17 |
23,564,307 (GRCm39) |
missense |
probably benign |
|
R9189:Vmn2r115
|
UTSW |
17 |
23,564,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R9351:Vmn2r115
|
UTSW |
17 |
23,578,482 (GRCm39) |
missense |
probably benign |
0.05 |
R9397:Vmn2r115
|
UTSW |
17 |
23,564,152 (GRCm39) |
nonsense |
probably null |
|
R9410:Vmn2r115
|
UTSW |
17 |
23,578,915 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9593:Vmn2r115
|
UTSW |
17 |
23,578,184 (GRCm39) |
missense |
probably damaging |
0.99 |
V5622:Vmn2r115
|
UTSW |
17 |
23,578,333 (GRCm39) |
missense |
probably benign |
|
V5622:Vmn2r115
|
UTSW |
17 |
23,565,201 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
X0033:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|