Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
G |
7: 119,953,701 (GRCm39) |
N535S |
probably benign |
Het |
Abcc6 |
A |
T |
7: 45,648,165 (GRCm39) |
L717Q |
probably benign |
Het |
Abraxas2 |
C |
A |
7: 132,484,790 (GRCm39) |
Q278K |
probably benign |
Het |
Acap2 |
A |
T |
16: 30,924,342 (GRCm39) |
D637E |
probably benign |
Het |
AI661453 |
A |
G |
17: 47,777,023 (GRCm39) |
|
probably benign |
Het |
Aoah |
A |
T |
13: 21,024,266 (GRCm39) |
E74V |
probably damaging |
Het |
Aoc1l1 |
A |
T |
6: 48,953,629 (GRCm39) |
D518V |
probably damaging |
Het |
Appl1 |
A |
G |
14: 26,671,576 (GRCm39) |
L292S |
possibly damaging |
Het |
Astl |
T |
A |
2: 127,189,109 (GRCm39) |
V166E |
probably damaging |
Het |
Bbs1 |
T |
G |
19: 4,953,735 (GRCm39) |
K143Q |
possibly damaging |
Het |
Bbx |
T |
C |
16: 50,094,907 (GRCm39) |
|
probably benign |
Het |
Birc6 |
A |
T |
17: 74,967,408 (GRCm39) |
Q4103L |
possibly damaging |
Het |
C1qtnf2 |
T |
G |
11: 43,381,811 (GRCm39) |
F178V |
probably damaging |
Het |
Camta2 |
A |
G |
11: 70,562,401 (GRCm39) |
F999L |
probably benign |
Het |
Cfap68 |
T |
C |
9: 50,676,174 (GRCm39) |
Y32C |
probably damaging |
Het |
Clcn7 |
A |
G |
17: 25,363,425 (GRCm39) |
I34V |
probably benign |
Het |
Cntn5 |
G |
T |
9: 9,748,420 (GRCm39) |
P487Q |
probably damaging |
Het |
Ctu2 |
T |
A |
8: 123,205,891 (GRCm39) |
I213K |
probably benign |
Het |
Des |
C |
A |
1: 75,340,108 (GRCm39) |
|
probably benign |
Het |
Dgcr8 |
A |
T |
16: 18,098,094 (GRCm39) |
D432E |
probably benign |
Het |
Dlgap5 |
G |
A |
14: 47,633,380 (GRCm39) |
R549* |
probably null |
Het |
Dmac2l |
A |
G |
12: 69,787,828 (GRCm39) |
Q88R |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,323,194 (GRCm39) |
T1397A |
probably damaging |
Het |
Dnmt1 |
T |
A |
9: 20,848,451 (GRCm39) |
|
probably benign |
Het |
Dstyk |
T |
A |
1: 132,391,113 (GRCm39) |
M838K |
probably damaging |
Het |
Dtwd1 |
C |
A |
2: 126,001,904 (GRCm39) |
T208N |
probably damaging |
Het |
Dvl1 |
G |
A |
4: 155,932,273 (GRCm39) |
V28I |
possibly damaging |
Het |
Dync1i2 |
T |
A |
2: 71,044,907 (GRCm39) |
|
probably benign |
Het |
Fer1l6 |
T |
A |
15: 58,499,383 (GRCm39) |
M1251K |
probably benign |
Het |
Fmod |
T |
C |
1: 133,968,256 (GRCm39) |
Y99H |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,645,163 (GRCm39) |
V1552D |
probably damaging |
Het |
Fnip2 |
A |
T |
3: 79,407,739 (GRCm39) |
S281T |
probably damaging |
Het |
Glb1 |
A |
G |
9: 114,293,233 (GRCm39) |
H536R |
probably benign |
Het |
Glis2 |
T |
A |
16: 4,431,506 (GRCm39) |
S344R |
possibly damaging |
Het |
Gm4847 |
A |
T |
1: 166,462,472 (GRCm39) |
S339R |
probably benign |
Het |
Gpr155 |
A |
G |
2: 73,187,002 (GRCm39) |
S44P |
probably benign |
Het |
Gprin1 |
G |
A |
13: 54,886,445 (GRCm39) |
P610S |
probably damaging |
Het |
Gvin3 |
T |
A |
7: 106,202,215 (GRCm39) |
H343L |
possibly damaging |
Het |
H2-Ob |
A |
T |
17: 34,461,554 (GRCm39) |
M98L |
probably benign |
Het |
H3c6 |
T |
C |
13: 23,746,530 (GRCm39) |
T4A |
probably benign |
Het |
Hmcn2 |
T |
C |
2: 31,223,943 (GRCm39) |
|
probably benign |
Het |
Ikbke |
C |
A |
1: 131,201,211 (GRCm39) |
V176L |
probably damaging |
Het |
Il13 |
T |
C |
11: 53,523,351 (GRCm39) |
T85A |
possibly damaging |
Het |
Inpp5k |
A |
T |
11: 75,538,017 (GRCm39) |
|
probably null |
Het |
Irgm2 |
T |
C |
11: 58,111,355 (GRCm39) |
S361P |
possibly damaging |
Het |
Itga11 |
C |
T |
9: 62,639,486 (GRCm39) |
|
probably benign |
Het |
Kalrn |
G |
T |
16: 33,829,632 (GRCm39) |
|
probably benign |
Het |
Kcng1 |
C |
A |
2: 168,110,952 (GRCm39) |
G71C |
probably damaging |
Het |
Kcnq5 |
T |
A |
1: 21,575,573 (GRCm39) |
D291V |
probably damaging |
Het |
Klhl7 |
A |
T |
5: 24,305,861 (GRCm39) |
M37L |
probably benign |
Het |
Letm1 |
A |
AG |
5: 33,926,859 (GRCm39) |
|
probably null |
Het |
Lhx6 |
C |
T |
2: 35,977,478 (GRCm39) |
V325I |
probably benign |
Het |
Lipc |
A |
G |
9: 70,841,817 (GRCm39) |
I9T |
possibly damaging |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Mast1 |
C |
A |
8: 85,648,107 (GRCm39) |
G458V |
probably damaging |
Het |
Mga |
T |
C |
2: 119,794,638 (GRCm39) |
V2565A |
possibly damaging |
Het |
Mpzl2 |
C |
G |
9: 44,955,471 (GRCm39) |
D127E |
probably benign |
Het |
Mrtfb |
T |
C |
16: 13,230,450 (GRCm39) |
I1045T |
probably damaging |
Het |
Myh3 |
T |
A |
11: 66,981,882 (GRCm39) |
C793S |
probably benign |
Het |
Nomo1 |
T |
C |
7: 45,715,928 (GRCm39) |
L765P |
probably damaging |
Het |
Nup210 |
A |
G |
6: 91,005,858 (GRCm39) |
I1335T |
possibly damaging |
Het |
Or52b3 |
T |
C |
7: 102,204,267 (GRCm39) |
|
probably null |
Het |
Oxr1 |
T |
A |
15: 41,683,340 (GRCm39) |
S254R |
probably damaging |
Het |
Pan3 |
A |
G |
5: 147,466,908 (GRCm39) |
I592V |
possibly damaging |
Het |
Pask |
C |
T |
1: 93,249,019 (GRCm39) |
A794T |
probably benign |
Het |
Pex2 |
T |
C |
3: 5,626,650 (GRCm39) |
E53G |
probably damaging |
Het |
Pfkfb2 |
T |
C |
1: 130,626,460 (GRCm39) |
T438A |
probably benign |
Het |
Phactr4 |
T |
C |
4: 132,098,095 (GRCm39) |
E391G |
probably damaging |
Het |
Pira2 |
A |
T |
7: 3,847,344 (GRCm39) |
L115Q |
probably damaging |
Het |
Pkhd1l1 |
A |
T |
15: 44,376,273 (GRCm39) |
|
probably null |
Het |
Pnlip |
A |
G |
19: 58,664,876 (GRCm39) |
S235G |
probably benign |
Het |
Prkd1 |
A |
G |
12: 50,536,694 (GRCm39) |
V130A |
possibly damaging |
Het |
Ptpn13 |
A |
G |
5: 103,703,999 (GRCm39) |
T1344A |
probably benign |
Het |
Ptprc |
T |
C |
1: 138,001,419 (GRCm39) |
Y780C |
probably damaging |
Het |
Pxn |
T |
A |
5: 115,690,815 (GRCm39) |
|
probably benign |
Het |
Rap1gap2 |
G |
A |
11: 74,316,802 (GRCm39) |
T245M |
probably damaging |
Het |
Rc3h1 |
G |
T |
1: 160,757,827 (GRCm39) |
K48N |
probably damaging |
Het |
Rfwd3 |
T |
C |
8: 112,009,245 (GRCm39) |
I444V |
probably benign |
Het |
Rictor |
C |
T |
15: 6,794,588 (GRCm39) |
R293C |
probably damaging |
Het |
Rif1 |
T |
A |
2: 52,001,412 (GRCm39) |
I1622N |
possibly damaging |
Het |
Rnf213 |
T |
C |
11: 119,306,019 (GRCm39) |
V609A |
probably benign |
Het |
Scgb1b2 |
G |
T |
7: 30,991,188 (GRCm39) |
|
probably benign |
Het |
Serac1 |
A |
T |
17: 6,101,060 (GRCm39) |
I448N |
probably damaging |
Het |
Sh3kbp1 |
C |
A |
X: 158,607,492 (GRCm39) |
T200K |
probably benign |
Het |
Sned1 |
T |
A |
1: 93,199,406 (GRCm39) |
F495L |
probably damaging |
Het |
Socs7 |
T |
C |
11: 97,263,950 (GRCm39) |
F281L |
probably benign |
Het |
Spta1 |
C |
T |
1: 174,040,180 (GRCm39) |
L1214F |
probably benign |
Het |
Ssu72 |
A |
G |
4: 155,789,900 (GRCm39) |
E21G |
probably damaging |
Het |
Syngr4 |
A |
G |
7: 45,536,464 (GRCm39) |
V186A |
probably benign |
Het |
Tars3 |
G |
A |
7: 65,305,539 (GRCm39) |
M254I |
possibly damaging |
Het |
Tmem130 |
C |
A |
5: 144,680,595 (GRCm39) |
V270L |
probably benign |
Het |
Trim66 |
A |
T |
7: 109,074,320 (GRCm39) |
I647N |
probably damaging |
Het |
Tspyl2 |
A |
T |
X: 151,121,890 (GRCm39) |
D572E |
probably benign |
Het |
Unc45b |
G |
A |
11: 82,808,580 (GRCm39) |
R222H |
probably benign |
Het |
Uxs1 |
T |
C |
1: 43,866,783 (GRCm39) |
Y29C |
probably damaging |
Het |
Vmn1r202 |
C |
T |
13: 22,685,953 (GRCm39) |
G155S |
possibly damaging |
Het |
Vmn2r24 |
T |
A |
6: 123,755,972 (GRCm39) |
F15I |
probably benign |
Het |
Wdr64 |
A |
G |
1: 175,594,661 (GRCm39) |
T471A |
probably benign |
Het |
Zfa-ps |
T |
A |
10: 52,419,373 (GRCm39) |
|
noncoding transcript |
Het |
Zfp260 |
A |
G |
7: 29,804,765 (GRCm39) |
K222E |
probably damaging |
Het |
Zfp300 |
A |
G |
X: 20,948,190 (GRCm39) |
S525P |
possibly damaging |
Het |
Zfp821 |
A |
G |
8: 110,450,979 (GRCm39) |
D324G |
probably damaging |
Het |
Zfp934 |
T |
C |
13: 62,665,648 (GRCm39) |
D331G |
probably damaging |
Het |
Zscan29 |
T |
C |
2: 121,000,587 (GRCm39) |
R7G |
probably damaging |
Het |
|
Other mutations in Virma |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00428:Virma
|
APN |
4 |
11,519,424 (GRCm39) |
splice site |
probably benign |
|
IGL00477:Virma
|
APN |
4 |
11,519,006 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01293:Virma
|
APN |
4 |
11,521,114 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01410:Virma
|
APN |
4 |
11,518,929 (GRCm39) |
nonsense |
probably null |
|
IGL01531:Virma
|
APN |
4 |
11,528,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01672:Virma
|
APN |
4 |
11,527,792 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01724:Virma
|
APN |
4 |
11,528,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01747:Virma
|
APN |
4 |
11,526,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01776:Virma
|
APN |
4 |
11,527,792 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02064:Virma
|
APN |
4 |
11,513,163 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02243:Virma
|
APN |
4 |
11,546,031 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02244:Virma
|
APN |
4 |
11,546,031 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02445:Virma
|
APN |
4 |
11,527,029 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02546:Virma
|
APN |
4 |
11,494,804 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02807:Virma
|
APN |
4 |
11,507,079 (GRCm39) |
splice site |
probably benign |
|
IGL02967:Virma
|
APN |
4 |
11,514,096 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03211:Virma
|
APN |
4 |
11,548,770 (GRCm39) |
nonsense |
probably null |
|
IGL03242:Virma
|
APN |
4 |
11,527,669 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03256:Virma
|
APN |
4 |
11,542,207 (GRCm39) |
splice site |
probably benign |
|
IGL03327:Virma
|
APN |
4 |
11,518,984 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03346:Virma
|
APN |
4 |
11,518,984 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4802001:Virma
|
UTSW |
4 |
11,546,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R0142:Virma
|
UTSW |
4 |
11,548,783 (GRCm39) |
missense |
probably benign |
0.04 |
R0355:Virma
|
UTSW |
4 |
11,528,626 (GRCm39) |
nonsense |
probably null |
|
R0522:Virma
|
UTSW |
4 |
11,519,416 (GRCm39) |
critical splice donor site |
probably null |
|
R0600:Virma
|
UTSW |
4 |
11,498,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R1435:Virma
|
UTSW |
4 |
11,528,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1489:Virma
|
UTSW |
4 |
11,521,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R1568:Virma
|
UTSW |
4 |
11,528,776 (GRCm39) |
missense |
probably damaging |
0.99 |
R1616:Virma
|
UTSW |
4 |
11,544,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R1655:Virma
|
UTSW |
4 |
11,494,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Virma
|
UTSW |
4 |
11,494,814 (GRCm39) |
missense |
probably damaging |
0.98 |
R1835:Virma
|
UTSW |
4 |
11,540,511 (GRCm39) |
missense |
probably benign |
0.02 |
R1951:Virma
|
UTSW |
4 |
11,513,907 (GRCm39) |
missense |
probably benign |
0.00 |
R1991:Virma
|
UTSW |
4 |
11,519,242 (GRCm39) |
missense |
probably benign |
0.06 |
R2172:Virma
|
UTSW |
4 |
11,527,843 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2217:Virma
|
UTSW |
4 |
11,544,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R2218:Virma
|
UTSW |
4 |
11,544,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Virma
|
UTSW |
4 |
11,518,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R2342:Virma
|
UTSW |
4 |
11,501,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R3424:Virma
|
UTSW |
4 |
11,513,177 (GRCm39) |
nonsense |
probably null |
|
R4397:Virma
|
UTSW |
4 |
11,513,901 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4449:Virma
|
UTSW |
4 |
11,498,828 (GRCm39) |
critical splice donor site |
probably null |
|
R4660:Virma
|
UTSW |
4 |
11,513,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R4698:Virma
|
UTSW |
4 |
11,528,636 (GRCm39) |
missense |
probably damaging |
0.99 |
R4878:Virma
|
UTSW |
4 |
11,544,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R4937:Virma
|
UTSW |
4 |
11,521,147 (GRCm39) |
nonsense |
probably null |
|
R5031:Virma
|
UTSW |
4 |
11,542,116 (GRCm39) |
nonsense |
probably null |
|
R5040:Virma
|
UTSW |
4 |
11,528,746 (GRCm39) |
missense |
probably benign |
0.01 |
R5061:Virma
|
UTSW |
4 |
11,494,840 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5091:Virma
|
UTSW |
4 |
11,519,392 (GRCm39) |
missense |
probably benign |
0.00 |
R5137:Virma
|
UTSW |
4 |
11,546,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R5262:Virma
|
UTSW |
4 |
11,539,926 (GRCm39) |
missense |
probably benign |
0.01 |
R5297:Virma
|
UTSW |
4 |
11,494,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R5730:Virma
|
UTSW |
4 |
11,542,154 (GRCm39) |
missense |
probably benign |
0.44 |
R5818:Virma
|
UTSW |
4 |
11,513,319 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5835:Virma
|
UTSW |
4 |
11,514,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R6125:Virma
|
UTSW |
4 |
11,521,172 (GRCm39) |
missense |
probably damaging |
0.98 |
R6197:Virma
|
UTSW |
4 |
11,505,498 (GRCm39) |
missense |
probably damaging |
0.96 |
R6222:Virma
|
UTSW |
4 |
11,527,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R6793:Virma
|
UTSW |
4 |
11,539,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R7028:Virma
|
UTSW |
4 |
11,519,249 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7356:Virma
|
UTSW |
4 |
11,513,595 (GRCm39) |
missense |
probably damaging |
0.99 |
R7383:Virma
|
UTSW |
4 |
11,514,026 (GRCm39) |
missense |
probably damaging |
0.98 |
R7391:Virma
|
UTSW |
4 |
11,508,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R7425:Virma
|
UTSW |
4 |
11,546,211 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7556:Virma
|
UTSW |
4 |
11,518,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R7715:Virma
|
UTSW |
4 |
11,513,016 (GRCm39) |
splice site |
probably null |
|
R7715:Virma
|
UTSW |
4 |
11,549,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Virma
|
UTSW |
4 |
11,540,023 (GRCm39) |
missense |
probably benign |
0.01 |
R7990:Virma
|
UTSW |
4 |
11,513,983 (GRCm39) |
missense |
probably benign |
0.00 |
R8048:Virma
|
UTSW |
4 |
11,539,918 (GRCm39) |
nonsense |
probably null |
|
R8050:Virma
|
UTSW |
4 |
11,528,643 (GRCm39) |
missense |
probably benign |
0.22 |
R8165:Virma
|
UTSW |
4 |
11,542,128 (GRCm39) |
missense |
probably benign |
0.00 |
R8412:Virma
|
UTSW |
4 |
11,521,261 (GRCm39) |
critical splice donor site |
probably null |
|
R8544:Virma
|
UTSW |
4 |
11,516,949 (GRCm39) |
missense |
probably benign |
|
R8551:Virma
|
UTSW |
4 |
11,513,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R8699:Virma
|
UTSW |
4 |
11,528,678 (GRCm39) |
missense |
probably benign |
0.04 |
R8739:Virma
|
UTSW |
4 |
11,540,643 (GRCm39) |
critical splice donor site |
probably null |
|
R8950:Virma
|
UTSW |
4 |
11,519,047 (GRCm39) |
nonsense |
probably null |
|
R9015:Virma
|
UTSW |
4 |
11,540,494 (GRCm39) |
missense |
probably benign |
0.27 |
R9038:Virma
|
UTSW |
4 |
11,526,922 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9115:Virma
|
UTSW |
4 |
11,498,744 (GRCm39) |
missense |
probably benign |
0.15 |
R9294:Virma
|
UTSW |
4 |
11,513,507 (GRCm39) |
nonsense |
probably null |
|
R9404:Virma
|
UTSW |
4 |
11,513,626 (GRCm39) |
missense |
probably benign |
0.17 |
R9477:Virma
|
UTSW |
4 |
11,528,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R9532:Virma
|
UTSW |
4 |
11,507,078 (GRCm39) |
critical splice donor site |
probably null |
|
R9649:Virma
|
UTSW |
4 |
11,486,045 (GRCm39) |
start codon destroyed |
probably null |
0.08 |
R9657:Virma
|
UTSW |
4 |
11,544,898 (GRCm39) |
missense |
probably damaging |
0.99 |
R9780:Virma
|
UTSW |
4 |
11,513,442 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9800:Virma
|
UTSW |
4 |
11,546,007 (GRCm39) |
missense |
probably damaging |
0.99 |
X0020:Virma
|
UTSW |
4 |
11,486,055 (GRCm39) |
missense |
probably benign |
0.00 |
|