Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
A |
7: 120,119,283 (GRCm39) |
I1009N |
possibly damaging |
Het |
Abtb3 |
C |
A |
10: 85,224,079 (GRCm39) |
A296E |
unknown |
Het |
Adcy8 |
T |
A |
15: 64,571,095 (GRCm39) |
N1213Y |
probably benign |
Het |
Ahctf1 |
T |
C |
1: 179,581,433 (GRCm39) |
S1590G |
possibly damaging |
Het |
Ahcyl1 |
A |
T |
3: 107,577,588 (GRCm39) |
N277K |
probably damaging |
Het |
Ank2 |
A |
T |
3: 126,740,149 (GRCm39) |
S1912T |
unknown |
Het |
Ank3 |
T |
A |
10: 69,733,957 (GRCm39) |
N740K |
unknown |
Het |
Atp13a3 |
A |
C |
16: 30,159,051 (GRCm39) |
I800S |
probably benign |
Het |
AU041133 |
T |
A |
10: 81,986,679 (GRCm39) |
C111S |
probably damaging |
Het |
Azi2 |
T |
A |
9: 117,884,924 (GRCm39) |
I211N |
probably benign |
Het |
Camk2b |
T |
C |
11: 5,922,408 (GRCm39) |
N480S |
probably damaging |
Het |
Card6 |
A |
G |
15: 5,128,702 (GRCm39) |
V898A |
probably benign |
Het |
Copb2 |
T |
A |
9: 98,461,081 (GRCm39) |
M381K |
probably damaging |
Het |
Cplx3 |
T |
C |
9: 57,523,060 (GRCm39) |
D133G |
probably damaging |
Het |
Crisp1 |
A |
T |
17: 40,616,071 (GRCm39) |
M102K |
probably damaging |
Het |
Dcxr |
A |
T |
11: 120,618,084 (GRCm39) |
|
probably benign |
Het |
Dennd5a |
C |
A |
7: 109,500,374 (GRCm39) |
R917L |
probably benign |
Het |
Egflam |
T |
A |
15: 7,279,525 (GRCm39) |
T494S |
probably benign |
Het |
Fkbpl |
T |
A |
17: 34,864,691 (GRCm39) |
M153K |
probably benign |
Het |
Helz2 |
A |
T |
2: 180,882,616 (GRCm39) |
I59N |
probably damaging |
Het |
Ldlrap1 |
T |
C |
4: 134,477,303 (GRCm39) |
T194A |
probably benign |
Het |
Lrrc27 |
T |
C |
7: 138,807,913 (GRCm39) |
M340T |
probably benign |
Het |
Lum |
T |
A |
10: 97,404,157 (GRCm39) |
S17R |
probably benign |
Het |
Malrd1 |
A |
G |
2: 15,847,405 (GRCm39) |
K1182E |
unknown |
Het |
Map3k2 |
A |
T |
18: 32,333,069 (GRCm39) |
D81V |
possibly damaging |
Het |
Muc5b |
A |
T |
7: 141,415,480 (GRCm39) |
T2809S |
possibly damaging |
Het |
Nle1 |
C |
A |
11: 82,793,876 (GRCm39) |
V387L |
probably benign |
Het |
Nr1h4 |
T |
C |
10: 89,290,618 (GRCm39) |
D474G |
probably benign |
Het |
Nup205 |
T |
C |
6: 35,163,468 (GRCm39) |
I144T |
possibly damaging |
Het |
Or10ag57 |
G |
T |
2: 87,218,508 (GRCm39) |
C153F |
probably damaging |
Het |
Or1e17 |
C |
A |
11: 73,831,986 (GRCm39) |
L305I |
probably benign |
Het |
Or2a56 |
A |
T |
6: 42,933,091 (GRCm39) |
I220F |
probably damaging |
Het |
Or4f15 |
G |
A |
2: 111,814,194 (GRCm39) |
S75L |
possibly damaging |
Het |
Or4n4 |
G |
A |
14: 50,519,701 (GRCm39) |
T3I |
probably benign |
Het |
Or51f1 |
T |
C |
7: 102,506,093 (GRCm39) |
Y132C |
probably benign |
Het |
Pkn3 |
C |
T |
2: 29,973,290 (GRCm39) |
R371* |
probably null |
Het |
Plin2 |
A |
T |
4: 86,586,742 (GRCm39) |
S30T |
possibly damaging |
Het |
Ppfibp1 |
T |
C |
6: 146,917,769 (GRCm39) |
V475A |
probably benign |
Het |
Ppp2ca |
T |
C |
11: 52,008,910 (GRCm39) |
Y137H |
probably damaging |
Het |
Rasgrf2 |
T |
A |
13: 92,267,860 (GRCm39) |
Q48L |
probably damaging |
Het |
Rnf168 |
G |
C |
16: 32,117,386 (GRCm39) |
V316L |
probably benign |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Spata31d1d |
T |
C |
13: 59,874,637 (GRCm39) |
H966R |
possibly damaging |
Het |
Speg |
C |
A |
1: 75,399,358 (GRCm39) |
D2268E |
probably benign |
Het |
Srp54c |
A |
G |
12: 55,296,811 (GRCm39) |
I170V |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,704,364 (GRCm39) |
R439G |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,949,558 (GRCm39) |
K1155R |
unknown |
Het |
Tmem184c |
T |
C |
8: 78,323,087 (GRCm39) |
I592V |
probably benign |
Het |
Trav6-7-dv9 |
A |
G |
14: 53,947,669 (GRCm39) |
Y57C |
probably damaging |
Het |
Trpc1 |
T |
A |
9: 95,625,303 (GRCm39) |
I108F |
probably damaging |
Het |
Vmn2r10 |
A |
T |
5: 109,150,404 (GRCm39) |
D213E |
probably damaging |
Het |
Vmn2r116 |
T |
A |
17: 23,620,399 (GRCm39) |
V711E |
probably damaging |
Het |
Vps16 |
T |
C |
2: 130,282,405 (GRCm39) |
F413L |
probably benign |
Het |
Vwa1 |
G |
A |
4: 155,857,336 (GRCm39) |
P154L |
probably damaging |
Het |
Wasf1 |
T |
C |
10: 40,812,693 (GRCm39) |
I494T |
unknown |
Het |
Wdr36 |
A |
G |
18: 32,985,700 (GRCm39) |
D539G |
possibly damaging |
Het |
Zfp81 |
A |
T |
17: 33,554,411 (GRCm39) |
C134* |
probably null |
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 |
R2145:Virma
|
UTSW |
4 |
11,548,726 (GRCm39) |
splice site |
probably benign |
|
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 |
X0020:Virma
|
UTSW |
4 |
11,486,055 (GRCm39) |
missense |
probably benign |
0.00 |
|