Other mutations in this stock |
Total: 150 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 |
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 |
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 |
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 Mpdz |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Mpdz
|
APN |
4 |
81,228,461 (GRCm39) |
nonsense |
probably null |
|
IGL00325:Mpdz
|
APN |
4 |
81,235,868 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00497:Mpdz
|
APN |
4 |
81,253,979 (GRCm39) |
missense |
probably benign |
0.30 |
IGL00502:Mpdz
|
APN |
4 |
81,287,960 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00539:Mpdz
|
APN |
4 |
81,279,588 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL00938:Mpdz
|
APN |
4 |
81,210,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01394:Mpdz
|
APN |
4 |
81,210,728 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01537:Mpdz
|
APN |
4 |
81,287,895 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01558:Mpdz
|
APN |
4 |
81,213,767 (GRCm39) |
nonsense |
probably null |
|
IGL01561:Mpdz
|
APN |
4 |
81,202,851 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01649:Mpdz
|
APN |
4 |
81,221,870 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01743:Mpdz
|
APN |
4 |
81,235,919 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Mpdz
|
APN |
4 |
81,204,624 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01969:Mpdz
|
APN |
4 |
81,276,961 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02023:Mpdz
|
APN |
4 |
81,247,766 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02081:Mpdz
|
APN |
4 |
81,254,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02304:Mpdz
|
APN |
4 |
81,215,796 (GRCm39) |
splice site |
probably benign |
|
IGL02304:Mpdz
|
APN |
4 |
81,228,394 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02410:Mpdz
|
APN |
4 |
81,215,730 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02449:Mpdz
|
APN |
4 |
81,247,659 (GRCm39) |
splice site |
probably null |
|
IGL02671:Mpdz
|
APN |
4 |
81,208,510 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Mpdz
|
APN |
4 |
81,202,808 (GRCm39) |
splice site |
probably null |
|
IGL02718:Mpdz
|
APN |
4 |
81,303,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03065:Mpdz
|
APN |
4 |
81,210,802 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03378:Mpdz
|
APN |
4 |
81,337,285 (GRCm39) |
splice site |
probably benign |
|
PIT4458001:Mpdz
|
UTSW |
4 |
81,337,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Mpdz
|
UTSW |
4 |
81,300,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Mpdz
|
UTSW |
4 |
81,300,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Mpdz
|
UTSW |
4 |
81,210,768 (GRCm39) |
missense |
probably benign |
0.44 |
R0402:Mpdz
|
UTSW |
4 |
81,279,677 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0499:Mpdz
|
UTSW |
4 |
81,210,768 (GRCm39) |
missense |
probably benign |
0.44 |
R0718:Mpdz
|
UTSW |
4 |
81,210,710 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0844:Mpdz
|
UTSW |
4 |
81,339,431 (GRCm39) |
start gained |
probably benign |
|
R0883:Mpdz
|
UTSW |
4 |
81,278,228 (GRCm39) |
splice site |
probably benign |
|
R0885:Mpdz
|
UTSW |
4 |
81,287,829 (GRCm39) |
missense |
probably benign |
0.04 |
R1344:Mpdz
|
UTSW |
4 |
81,226,556 (GRCm39) |
missense |
probably benign |
0.01 |
R1432:Mpdz
|
UTSW |
4 |
81,210,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Mpdz
|
UTSW |
4 |
81,266,945 (GRCm39) |
nonsense |
probably null |
|
R1589:Mpdz
|
UTSW |
4 |
81,339,413 (GRCm39) |
missense |
probably benign |
0.00 |
R1756:Mpdz
|
UTSW |
4 |
81,225,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1940:Mpdz
|
UTSW |
4 |
81,279,680 (GRCm39) |
missense |
probably benign |
0.01 |
R2068:Mpdz
|
UTSW |
4 |
81,254,067 (GRCm39) |
missense |
probably null |
1.00 |
R2182:Mpdz
|
UTSW |
4 |
81,266,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R2213:Mpdz
|
UTSW |
4 |
81,228,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R2265:Mpdz
|
UTSW |
4 |
81,301,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R2268:Mpdz
|
UTSW |
4 |
81,301,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Mpdz
|
UTSW |
4 |
81,301,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R3082:Mpdz
|
UTSW |
4 |
81,203,695 (GRCm39) |
splice site |
probably benign |
|
R3746:Mpdz
|
UTSW |
4 |
81,281,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R3902:Mpdz
|
UTSW |
4 |
81,225,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4095:Mpdz
|
UTSW |
4 |
81,302,060 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4097:Mpdz
|
UTSW |
4 |
81,253,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R4206:Mpdz
|
UTSW |
4 |
81,299,999 (GRCm39) |
missense |
probably benign |
0.13 |
R4675:Mpdz
|
UTSW |
4 |
81,302,049 (GRCm39) |
missense |
probably damaging |
0.98 |
R4884:Mpdz
|
UTSW |
4 |
81,279,713 (GRCm39) |
missense |
probably damaging |
0.97 |
R5044:Mpdz
|
UTSW |
4 |
81,299,934 (GRCm39) |
missense |
probably benign |
0.16 |
R5050:Mpdz
|
UTSW |
4 |
81,213,685 (GRCm39) |
missense |
probably benign |
0.00 |
R5243:Mpdz
|
UTSW |
4 |
81,225,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R5332:Mpdz
|
UTSW |
4 |
81,210,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R5435:Mpdz
|
UTSW |
4 |
81,201,724 (GRCm39) |
intron |
probably benign |
|
R5720:Mpdz
|
UTSW |
4 |
81,205,931 (GRCm39) |
missense |
probably damaging |
0.99 |
R5743:Mpdz
|
UTSW |
4 |
81,339,425 (GRCm39) |
start codon destroyed |
probably null |
0.30 |
R5764:Mpdz
|
UTSW |
4 |
81,274,683 (GRCm39) |
missense |
probably benign |
0.13 |
R5876:Mpdz
|
UTSW |
4 |
81,203,711 (GRCm39) |
nonsense |
probably null |
|
R5938:Mpdz
|
UTSW |
4 |
81,202,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Mpdz
|
UTSW |
4 |
81,202,812 (GRCm39) |
critical splice donor site |
probably null |
|
R6125:Mpdz
|
UTSW |
4 |
81,215,764 (GRCm39) |
missense |
probably benign |
0.00 |
R6178:Mpdz
|
UTSW |
4 |
81,226,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Mpdz
|
UTSW |
4 |
81,303,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R6293:Mpdz
|
UTSW |
4 |
81,278,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R6387:Mpdz
|
UTSW |
4 |
81,299,946 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6488:Mpdz
|
UTSW |
4 |
81,205,970 (GRCm39) |
missense |
probably benign |
0.11 |
R6536:Mpdz
|
UTSW |
4 |
81,301,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R6673:Mpdz
|
UTSW |
4 |
81,274,667 (GRCm39) |
missense |
probably benign |
0.11 |
R6879:Mpdz
|
UTSW |
4 |
81,266,893 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7180:Mpdz
|
UTSW |
4 |
81,253,988 (GRCm39) |
missense |
probably damaging |
0.98 |
R7199:Mpdz
|
UTSW |
4 |
81,215,570 (GRCm39) |
missense |
probably damaging |
0.98 |
R7209:Mpdz
|
UTSW |
4 |
81,225,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7309:Mpdz
|
UTSW |
4 |
81,300,195 (GRCm39) |
splice site |
probably null |
|
R7359:Mpdz
|
UTSW |
4 |
81,274,632 (GRCm39) |
missense |
probably benign |
0.01 |
R7561:Mpdz
|
UTSW |
4 |
81,225,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R7565:Mpdz
|
UTSW |
4 |
81,221,891 (GRCm39) |
missense |
probably benign |
0.01 |
R7738:Mpdz
|
UTSW |
4 |
81,253,986 (GRCm39) |
missense |
probably benign |
0.01 |
R7941:Mpdz
|
UTSW |
4 |
81,200,987 (GRCm39) |
missense |
probably benign |
0.04 |
R8074:Mpdz
|
UTSW |
4 |
81,267,324 (GRCm39) |
missense |
probably benign |
0.00 |
R8957:Mpdz
|
UTSW |
4 |
81,251,216 (GRCm39) |
nonsense |
probably null |
|
R8998:Mpdz
|
UTSW |
4 |
81,202,882 (GRCm39) |
nonsense |
probably null |
|
R8999:Mpdz
|
UTSW |
4 |
81,202,882 (GRCm39) |
nonsense |
probably null |
|
R9001:Mpdz
|
UTSW |
4 |
81,299,999 (GRCm39) |
missense |
probably benign |
|
R9223:Mpdz
|
UTSW |
4 |
81,202,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R9415:Mpdz
|
UTSW |
4 |
81,235,905 (GRCm39) |
nonsense |
probably null |
|
R9486:Mpdz
|
UTSW |
4 |
81,254,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R9520:Mpdz
|
UTSW |
4 |
81,304,555 (GRCm39) |
missense |
probably benign |
|
R9526:Mpdz
|
UTSW |
4 |
81,274,653 (GRCm39) |
missense |
probably benign |
|
R9556:Mpdz
|
UTSW |
4 |
81,278,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R9722:Mpdz
|
UTSW |
4 |
81,304,504 (GRCm39) |
missense |
probably damaging |
0.97 |
RF013:Mpdz
|
UTSW |
4 |
81,211,829 (GRCm39) |
missense |
possibly damaging |
0.60 |
X0011:Mpdz
|
UTSW |
4 |
81,210,996 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Mpdz
|
UTSW |
4 |
81,238,727 (GRCm39) |
missense |
probably damaging |
0.99 |
|