Other mutations in this stock |
Total: 149 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 |
C |
T |
11: 3,085,671 (GRCm39) |
A853T |
probably damaging |
Het |
Sfi1 |
T |
C |
11: 3,093,689 (GRCm39) |
|
probably benign |
Het |
Sfi1 |
G |
A |
11: 3,084,337 (GRCm39) |
A975V |
probably benign |
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 |
G |
A |
1: 85,553,854 (GRCm39) |
R231K |
probably benign |
Het |
Sp140 |
C |
T |
1: 85,553,886 (GRCm39) |
R242C |
possibly damaging |
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 |
Vmn2r115 |
G |
A |
17: 23,578,753 (GRCm39) |
G742D |
probably damaging |
Het |
Vmn2r115 |
C |
T |
17: 23,565,238 (GRCm39) |
S375F |
probably benign |
Het |
Vmn2r115 |
A |
G |
17: 23,575,934 (GRCm39) |
M511V |
probably benign |
Het |
Vmn2r115 |
A |
G |
17: 23,565,346 (GRCm39) |
Q411R |
probably benign |
Het |
Vmn2r115 |
C |
T |
17: 23,565,345 (GRCm39) |
Q411* |
probably null |
Het |
Vmn2r115 |
C |
T |
17: 23,578,371 (GRCm39) |
P615S |
probably damaging |
Het |
Vmn2r115 |
A |
G |
17: 23,565,135 (GRCm39) |
N341D |
probably benign |
Het |
Vmn2r115 |
G |
A |
17: 23,565,252 (GRCm39) |
E380K |
probably benign |
Het |
Vmn2r115 |
A |
C |
17: 23,565,313 (GRCm39) |
N400T |
probably damaging |
Het |
Vmn2r115 |
T |
A |
17: 23,578,798 (GRCm39) |
L757Q |
probably damaging |
Het |
Vmn2r115 |
G |
T |
17: 23,567,008 (GRCm39) |
G507* |
probably null |
Het |
Vmn2r115 |
A |
T |
17: 23,565,180 (GRCm39) |
M356L |
possibly damaging |
Het |
Vmn2r115 |
C |
T |
17: 23,565,150 (GRCm39) |
P346S |
probably benign |
Het |
Vmn2r115 |
G |
T |
17: 23,578,323 (GRCm39) |
A599S |
probably benign |
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 |
G |
X: 123,037,499 (GRCm39) |
K840N |
probably benign |
Het |
Vmn2r121 |
C |
T |
X: 123,043,413 (GRCm39) |
E73K |
probably benign |
Het |
Vmn2r121 |
T |
A |
X: 123,037,480 (GRCm39) |
N847Y |
possibly damaging |
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 |
Vmn2r125 |
T |
C |
4: 156,703,678 (GRCm39) |
M352T |
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 Vmn2r116 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00898:Vmn2r116
|
APN |
17 |
23,604,969 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00985:Vmn2r116
|
APN |
17 |
23,620,489 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Vmn2r116
|
APN |
17 |
23,606,210 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01383:Vmn2r116
|
APN |
17 |
23,620,575 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01459:Vmn2r116
|
APN |
17 |
23,603,903 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01725:Vmn2r116
|
APN |
17 |
23,605,619 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02125:Vmn2r116
|
APN |
17 |
23,616,601 (GRCm39) |
splice site |
probably benign |
|
IGL02170:Vmn2r116
|
APN |
17 |
23,603,907 (GRCm39) |
missense |
probably benign |
|
IGL02209:Vmn2r116
|
APN |
17 |
23,607,761 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02226:Vmn2r116
|
APN |
17 |
23,603,808 (GRCm39) |
missense |
probably null |
|
IGL02272:Vmn2r116
|
APN |
17 |
23,604,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02272:Vmn2r116
|
APN |
17 |
23,604,973 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02403:Vmn2r116
|
APN |
17 |
23,606,338 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02686:Vmn2r116
|
APN |
17 |
23,607,767 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02750:Vmn2r116
|
APN |
17 |
23,616,608 (GRCm39) |
splice site |
probably benign |
|
IGL02977:Vmn2r116
|
APN |
17 |
23,607,748 (GRCm39) |
missense |
possibly damaging |
0.90 |
PIT4449001:Vmn2r116
|
UTSW |
17 |
23,607,921 (GRCm39) |
missense |
probably benign |
0.41 |
R0015:Vmn2r116
|
UTSW |
17 |
23,620,823 (GRCm39) |
missense |
probably benign |
0.03 |
R0219:Vmn2r116
|
UTSW |
17 |
23,605,072 (GRCm39) |
nonsense |
probably null |
|
R0281:Vmn2r116
|
UTSW |
17 |
23,620,387 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0415:Vmn2r116
|
UTSW |
17 |
23,606,253 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0592:Vmn2r116
|
UTSW |
17 |
23,605,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R0610:Vmn2r116
|
UTSW |
17 |
23,606,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Vmn2r116
|
UTSW |
17 |
23,605,861 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0843:Vmn2r116
|
UTSW |
17 |
23,619,934 (GRCm39) |
missense |
probably benign |
0.01 |
R1329:Vmn2r116
|
UTSW |
17 |
23,606,162 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1396:Vmn2r116
|
UTSW |
17 |
23,605,115 (GRCm39) |
missense |
probably benign |
|
R1401:Vmn2r116
|
UTSW |
17 |
23,605,570 (GRCm39) |
splice site |
probably benign |
|
R1574:Vmn2r116
|
UTSW |
17 |
23,606,063 (GRCm39) |
missense |
probably damaging |
0.99 |
R1574:Vmn2r116
|
UTSW |
17 |
23,606,063 (GRCm39) |
missense |
probably damaging |
0.99 |
R1766:Vmn2r116
|
UTSW |
17 |
23,620,740 (GRCm39) |
missense |
probably damaging |
0.98 |
R2157:Vmn2r116
|
UTSW |
17 |
23,620,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R3622:Vmn2r116
|
UTSW |
17 |
23,605,025 (GRCm39) |
missense |
probably benign |
0.11 |
R3690:Vmn2r116
|
UTSW |
17 |
23,603,798 (GRCm39) |
missense |
unknown |
|
R4298:Vmn2r116
|
UTSW |
17 |
23,620,801 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4373:Vmn2r116
|
UTSW |
17 |
23,620,395 (GRCm39) |
missense |
probably benign |
0.01 |
R4860:Vmn2r116
|
UTSW |
17 |
23,620,777 (GRCm39) |
missense |
probably benign |
|
R4941:Vmn2r116
|
UTSW |
17 |
23,620,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R5119:Vmn2r116
|
UTSW |
17 |
23,606,138 (GRCm39) |
missense |
probably benign |
0.01 |
R5503:Vmn2r116
|
UTSW |
17 |
23,605,778 (GRCm39) |
missense |
probably benign |
0.07 |
R5510:Vmn2r116
|
UTSW |
17 |
23,605,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Vmn2r116
|
UTSW |
17 |
23,620,041 (GRCm39) |
missense |
probably benign |
0.00 |
R5689:Vmn2r116
|
UTSW |
17 |
23,616,693 (GRCm39) |
missense |
probably benign |
0.30 |
R5765:Vmn2r116
|
UTSW |
17 |
23,620,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R5794:Vmn2r116
|
UTSW |
17 |
23,604,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R5807:Vmn2r116
|
UTSW |
17 |
23,606,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R5837:Vmn2r116
|
UTSW |
17 |
23,606,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6262:Vmn2r116
|
UTSW |
17 |
23,606,351 (GRCm39) |
missense |
probably benign |
0.03 |
R6298:Vmn2r116
|
UTSW |
17 |
23,605,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R6651:Vmn2r116
|
UTSW |
17 |
23,607,805 (GRCm39) |
nonsense |
probably null |
|
R6667:Vmn2r116
|
UTSW |
17 |
23,620,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R7393:Vmn2r116
|
UTSW |
17 |
23,605,099 (GRCm39) |
missense |
probably benign |
0.14 |
R7571:Vmn2r116
|
UTSW |
17 |
23,603,830 (GRCm39) |
splice site |
probably null |
|
R7940:Vmn2r116
|
UTSW |
17 |
23,605,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R8510:Vmn2r116
|
UTSW |
17 |
23,604,905 (GRCm39) |
nonsense |
probably null |
|
R8950:Vmn2r116
|
UTSW |
17 |
23,620,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R8956:Vmn2r116
|
UTSW |
17 |
23,605,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R8977:Vmn2r116
|
UTSW |
17 |
23,605,916 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9030:Vmn2r116
|
UTSW |
17 |
23,603,864 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9077:Vmn2r116
|
UTSW |
17 |
23,604,956 (GRCm39) |
missense |
probably benign |
0.14 |
R9223:Vmn2r116
|
UTSW |
17 |
23,620,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Vmn2r116
|
UTSW |
17 |
23,620,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R9449:Vmn2r116
|
UTSW |
17 |
23,605,919 (GRCm39) |
missense |
probably benign |
0.01 |
R9746:Vmn2r116
|
UTSW |
17 |
23,620,797 (GRCm39) |
missense |
probably benign |
0.08 |
R9755:Vmn2r116
|
UTSW |
17 |
23,620,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R9759:Vmn2r116
|
UTSW |
17 |
23,620,360 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9800:Vmn2r116
|
UTSW |
17 |
23,620,399 (GRCm39) |
missense |
probably damaging |
0.97 |
S24628:Vmn2r116
|
UTSW |
17 |
23,606,253 (GRCm39) |
missense |
possibly damaging |
0.55 |
Z1176:Vmn2r116
|
UTSW |
17 |
23,620,402 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Vmn2r116
|
UTSW |
17 |
23,607,866 (GRCm39) |
missense |
probably benign |
|
|