Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
A2m |
A |
G |
6: 121,616,295 (GRCm39) |
K141R |
probably damaging |
Het |
Ablim3 |
T |
C |
18: 61,956,993 (GRCm39) |
E278G |
probably damaging |
Het |
Adam28 |
A |
G |
14: 68,893,130 (GRCm39) |
W4R |
possibly damaging |
Het |
Ahnak2 |
T |
C |
12: 112,742,230 (GRCm39) |
N614S |
possibly damaging |
Het |
Arfgef1 |
A |
G |
1: 10,230,964 (GRCm39) |
S1182P |
probably damaging |
Het |
Asb8 |
A |
T |
15: 98,034,263 (GRCm39) |
D97E |
probably damaging |
Het |
AU041133 |
T |
A |
10: 81,987,046 (GRCm39) |
L232H |
probably damaging |
Het |
Bmp2k |
T |
G |
5: 97,204,841 (GRCm39) |
V392G |
possibly damaging |
Het |
Capn12 |
C |
A |
7: 28,581,383 (GRCm39) |
H79N |
probably benign |
Het |
Casp2 |
C |
A |
6: 42,244,520 (GRCm39) |
S54R |
possibly damaging |
Het |
Ccdc18 |
T |
C |
5: 108,288,740 (GRCm39) |
S163P |
possibly damaging |
Het |
Ccdc92b |
A |
G |
11: 74,528,838 (GRCm39) |
E114G |
probably benign |
Het |
Cd209c |
C |
A |
8: 3,995,699 (GRCm39) |
M34I |
probably benign |
Het |
Ceacam18 |
A |
T |
7: 43,286,382 (GRCm39) |
H85L |
probably benign |
Het |
Cndp1 |
C |
A |
18: 84,630,958 (GRCm39) |
A434S |
probably benign |
Het |
Crybg1 |
T |
A |
10: 43,851,129 (GRCm39) |
T1581S |
probably benign |
Het |
Cyb5d2 |
A |
T |
11: 72,680,036 (GRCm39) |
D86E |
probably damaging |
Het |
Duox1 |
T |
G |
2: 122,158,341 (GRCm39) |
V608G |
probably benign |
Het |
Exosc10 |
A |
G |
4: 148,649,844 (GRCm39) |
R425G |
probably damaging |
Het |
Fat3 |
A |
T |
9: 16,287,129 (GRCm39) |
I798N |
probably damaging |
Het |
Habp2 |
T |
A |
19: 56,295,218 (GRCm39) |
D36E |
probably benign |
Het |
Herpud1 |
T |
C |
8: 95,118,867 (GRCm39) |
V207A |
probably damaging |
Het |
Htt |
A |
G |
5: 34,970,534 (GRCm39) |
I561V |
probably benign |
Het |
Hyls1 |
G |
A |
9: 35,472,480 (GRCm39) |
S312F |
probably benign |
Het |
Igkv18-36 |
A |
G |
6: 69,969,512 (GRCm39) |
I93T |
probably damaging |
Het |
Kalrn |
T |
G |
16: 33,807,461 (GRCm39) |
E2636A |
probably benign |
Het |
Kif27 |
A |
G |
13: 58,460,960 (GRCm39) |
|
probably null |
Het |
Mep1a |
G |
A |
17: 43,789,055 (GRCm39) |
H574Y |
probably benign |
Het |
Myh6 |
T |
C |
14: 55,187,864 (GRCm39) |
K1197E |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,892,907 (GRCm39) |
T6780A |
probably benign |
Het |
Obscn |
C |
T |
11: 58,932,953 (GRCm39) |
V4808M |
probably damaging |
Het |
Or6c210 |
A |
G |
10: 129,495,803 (GRCm39) |
I43V |
probably benign |
Het |
Pkhd1 |
T |
C |
1: 20,271,307 (GRCm39) |
D3082G |
probably benign |
Het |
Plch1 |
T |
C |
3: 63,604,943 (GRCm39) |
M1645V |
probably benign |
Het |
Ppip5k1 |
A |
G |
2: 121,168,380 (GRCm39) |
V674A |
probably benign |
Het |
Prrc2b |
T |
A |
2: 32,096,485 (GRCm39) |
S619T |
probably benign |
Het |
Rab44 |
A |
T |
17: 29,367,212 (GRCm39) |
H714L |
probably benign |
Het |
Rybp |
A |
G |
6: 100,210,151 (GRCm39) |
Y70H |
possibly damaging |
Het |
Sfrp1 |
A |
G |
8: 23,936,260 (GRCm39) |
K234R |
possibly damaging |
Het |
Slc1a2 |
A |
G |
2: 102,607,795 (GRCm39) |
N481S |
probably damaging |
Het |
Slc44a3 |
T |
G |
3: 121,320,849 (GRCm39) |
I51L |
probably benign |
Het |
Slitrk1 |
A |
G |
14: 109,149,004 (GRCm39) |
F569S |
possibly damaging |
Het |
Smurf2 |
A |
T |
11: 106,726,974 (GRCm39) |
N451K |
probably damaging |
Het |
Sptbn2 |
T |
A |
19: 4,788,247 (GRCm39) |
D1075E |
probably damaging |
Het |
Syngap1 |
A |
T |
17: 27,177,192 (GRCm39) |
H65L |
probably benign |
Het |
Tdrd12 |
T |
C |
7: 35,228,689 (GRCm39) |
D11G |
probably damaging |
Het |
Tex2 |
C |
T |
11: 106,410,739 (GRCm39) |
A926T |
unknown |
Het |
Tm7sf2 |
A |
G |
19: 6,113,914 (GRCm39) |
F209S |
probably damaging |
Het |
Trbv12-2 |
G |
A |
6: 41,095,774 (GRCm39) |
|
probably benign |
Het |
Virma |
T |
A |
4: 11,514,036 (GRCm39) |
L630H |
probably damaging |
Het |
Zan |
C |
A |
5: 137,454,917 (GRCm39) |
R1373L |
unknown |
Het |
|
Other mutations in Vmn1r68 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01892:Vmn1r68
|
APN |
7 |
10,261,334 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02051:Vmn1r68
|
APN |
7 |
10,261,948 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02112:Vmn1r68
|
APN |
7 |
10,261,787 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02619:Vmn1r68
|
APN |
7 |
10,261,603 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03033:Vmn1r68
|
APN |
7 |
10,262,074 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03184:Vmn1r68
|
APN |
7 |
10,261,799 (GRCm39) |
missense |
probably benign |
0.16 |
PIT4354001:Vmn1r68
|
UTSW |
7 |
10,261,958 (GRCm39) |
missense |
probably benign |
|
R0141:Vmn1r68
|
UTSW |
7 |
10,261,252 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0359:Vmn1r68
|
UTSW |
7 |
10,261,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R0634:Vmn1r68
|
UTSW |
7 |
10,261,162 (GRCm39) |
missense |
probably benign |
0.00 |
R1731:Vmn1r68
|
UTSW |
7 |
10,261,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R2021:Vmn1r68
|
UTSW |
7 |
10,261,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2022:Vmn1r68
|
UTSW |
7 |
10,261,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2243:Vmn1r68
|
UTSW |
7 |
10,262,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R2262:Vmn1r68
|
UTSW |
7 |
10,261,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R3877:Vmn1r68
|
UTSW |
7 |
10,261,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Vmn1r68
|
UTSW |
7 |
10,261,275 (GRCm39) |
missense |
probably benign |
0.23 |
R4843:Vmn1r68
|
UTSW |
7 |
10,261,904 (GRCm39) |
missense |
probably benign |
0.00 |
R5198:Vmn1r68
|
UTSW |
7 |
10,261,723 (GRCm39) |
missense |
probably benign |
0.00 |
R5906:Vmn1r68
|
UTSW |
7 |
10,261,550 (GRCm39) |
missense |
probably benign |
0.02 |
R6015:Vmn1r68
|
UTSW |
7 |
10,261,616 (GRCm39) |
missense |
probably benign |
0.31 |
R7073:Vmn1r68
|
UTSW |
7 |
10,261,778 (GRCm39) |
missense |
probably benign |
0.00 |
R7614:Vmn1r68
|
UTSW |
7 |
10,261,553 (GRCm39) |
missense |
probably benign |
0.05 |
R7699:Vmn1r68
|
UTSW |
7 |
10,261,559 (GRCm39) |
missense |
probably benign |
0.15 |
R7700:Vmn1r68
|
UTSW |
7 |
10,261,559 (GRCm39) |
missense |
probably benign |
0.15 |
R7912:Vmn1r68
|
UTSW |
7 |
10,261,237 (GRCm39) |
missense |
probably benign |
0.01 |
R8166:Vmn1r68
|
UTSW |
7 |
10,261,888 (GRCm39) |
missense |
probably benign |
0.10 |
R8426:Vmn1r68
|
UTSW |
7 |
10,261,382 (GRCm39) |
missense |
probably benign |
0.02 |
R9466:Vmn1r68
|
UTSW |
7 |
10,261,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R9466:Vmn1r68
|
UTSW |
7 |
10,261,317 (GRCm39) |
nonsense |
probably null |
|
|