Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat1 |
T |
C |
8: 112,709,128 (GRCm39) |
K232E |
probably benign |
Het |
Apba1 |
T |
C |
19: 23,871,326 (GRCm39) |
M386T |
probably damaging |
Het |
Appl2 |
G |
T |
10: 83,444,601 (GRCm39) |
F472L |
possibly damaging |
Het |
Atxn2 |
T |
C |
5: 121,941,140 (GRCm39) |
Y56H |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,647,368 (GRCm39) |
Y809C |
probably damaging |
Het |
Canx |
C |
T |
11: 50,201,694 (GRCm39) |
V59I |
probably benign |
Het |
Catsperb |
T |
C |
12: 101,560,478 (GRCm39) |
L823P |
probably damaging |
Het |
Crb3 |
T |
C |
17: 57,372,090 (GRCm39) |
S46P |
probably benign |
Het |
Daam1 |
G |
A |
12: 72,036,601 (GRCm39) |
R1058H |
probably damaging |
Het |
Ehd1 |
T |
A |
19: 6,348,502 (GRCm39) |
D493E |
probably damaging |
Het |
Eml6 |
T |
A |
11: 29,768,907 (GRCm39) |
Q746L |
probably damaging |
Het |
Epg5 |
T |
A |
18: 77,992,287 (GRCm39) |
M328K |
probably benign |
Het |
Flt4 |
T |
A |
11: 49,515,555 (GRCm39) |
S48T |
probably benign |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably null |
Het |
Gm7535 |
A |
G |
17: 18,131,936 (GRCm39) |
|
probably benign |
Het |
Gpat4 |
G |
A |
8: 23,670,171 (GRCm39) |
P286L |
probably damaging |
Het |
Hmcn2 |
A |
T |
2: 31,240,586 (GRCm39) |
T494S |
probably benign |
Het |
Hydin |
G |
A |
8: 111,145,138 (GRCm39) |
V830I |
probably benign |
Het |
Map3k6 |
T |
A |
4: 132,973,983 (GRCm39) |
H487Q |
possibly damaging |
Het |
Myh14 |
G |
A |
7: 44,283,800 (GRCm39) |
P735S |
probably damaging |
Het |
Nfkb2 |
T |
C |
19: 46,296,163 (GRCm39) |
|
probably null |
Het |
Nlrp4c |
T |
C |
7: 6,076,113 (GRCm39) |
V671A |
probably benign |
Het |
Nsrp1 |
A |
T |
11: 76,936,587 (GRCm39) |
Y536* |
probably null |
Het |
Or4c112 |
G |
T |
2: 88,853,770 (GRCm39) |
H192Q |
probably benign |
Het |
Pak5 |
A |
G |
2: 135,958,123 (GRCm39) |
S322P |
probably damaging |
Het |
Pank2 |
A |
G |
2: 131,124,601 (GRCm39) |
|
probably null |
Het |
Phf6 |
A |
T |
X: 52,031,525 (GRCm39) |
I272F |
probably damaging |
Het |
Plxna2 |
T |
C |
1: 194,480,056 (GRCm39) |
L1409P |
probably damaging |
Het |
Polr2a |
A |
G |
11: 69,633,511 (GRCm39) |
|
probably null |
Het |
Pp2d1 |
C |
A |
17: 53,822,482 (GRCm39) |
V195L |
probably benign |
Het |
Psma1 |
C |
T |
7: 113,864,173 (GRCm39) |
E227K |
unknown |
Het |
Ptger1 |
C |
T |
8: 84,395,357 (GRCm39) |
T278I |
probably benign |
Het |
Slc20a2 |
C |
A |
8: 23,050,532 (GRCm39) |
S250R |
probably benign |
Het |
Slc27a2 |
A |
G |
2: 126,409,672 (GRCm39) |
T285A |
probably damaging |
Het |
Slc47a2 |
T |
C |
11: 61,204,497 (GRCm39) |
T285A |
probably benign |
Het |
Slf1 |
T |
A |
13: 77,194,825 (GRCm39) |
|
probably null |
Het |
Tiam2 |
A |
G |
17: 3,465,389 (GRCm39) |
T373A |
probably benign |
Het |
Timd2 |
T |
A |
11: 46,577,844 (GRCm39) |
I96L |
probably damaging |
Het |
Tmem59l |
A |
G |
8: 70,939,951 (GRCm39) |
L6S |
unknown |
Het |
Tmem64 |
T |
C |
4: 15,266,658 (GRCm39) |
I236T |
possibly damaging |
Het |
Trpm2 |
T |
A |
10: 77,777,016 (GRCm39) |
D427V |
probably damaging |
Het |
Vax2 |
A |
T |
6: 83,714,871 (GRCm39) |
Y262F |
probably damaging |
Het |
Zan |
C |
A |
5: 137,408,568 (GRCm39) |
|
probably benign |
Het |
Zbtb22 |
T |
G |
17: 34,136,939 (GRCm39) |
D361E |
probably damaging |
Het |
Zfp27 |
A |
G |
7: 29,595,536 (GRCm39) |
L143P |
possibly 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 |
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 |
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 |
|