Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9030624G23Rik |
T |
C |
12: 24,124,417 (GRCm39) |
Y86C |
probably benign |
Het |
Adgra2 |
G |
A |
8: 27,607,535 (GRCm39) |
V47M |
probably damaging |
Het |
Anks1b |
T |
C |
10: 89,912,921 (GRCm39) |
C349R |
possibly damaging |
Het |
Anks4b |
A |
T |
7: 119,781,914 (GRCm39) |
|
probably benign |
Het |
Apobec2 |
A |
G |
17: 48,730,295 (GRCm39) |
S124P |
probably damaging |
Het |
Brd8 |
G |
A |
18: 34,740,354 (GRCm39) |
S493L |
probably benign |
Het |
Cbln3 |
A |
G |
14: 56,120,944 (GRCm39) |
Y126H |
probably damaging |
Het |
Ccdc138 |
T |
C |
10: 58,364,721 (GRCm39) |
|
probably benign |
Het |
Cckbr |
C |
T |
7: 105,083,238 (GRCm39) |
A147V |
probably damaging |
Het |
Ceacam2 |
T |
A |
7: 25,219,411 (GRCm39) |
H283L |
probably damaging |
Het |
Cfap251 |
A |
G |
5: 123,392,699 (GRCm39) |
|
probably benign |
Het |
Clasp1 |
A |
G |
1: 118,478,834 (GRCm39) |
D718G |
possibly damaging |
Het |
Clmn |
A |
T |
12: 104,739,493 (GRCm39) |
Y979N |
probably damaging |
Het |
Dennd5b |
T |
C |
6: 148,920,840 (GRCm39) |
R851G |
probably null |
Het |
Dock1 |
T |
C |
7: 134,768,944 (GRCm39) |
V1771A |
probably benign |
Het |
Dysf |
T |
A |
6: 84,077,187 (GRCm39) |
L694Q |
probably damaging |
Het |
Faim2 |
T |
C |
15: 99,419,138 (GRCm39) |
Y77C |
probably benign |
Het |
Fbxw22 |
A |
T |
9: 109,215,732 (GRCm39) |
I172N |
probably damaging |
Het |
Fhad1 |
C |
T |
4: 141,646,069 (GRCm39) |
D298N |
probably benign |
Het |
Fyb1 |
T |
G |
15: 6,688,040 (GRCm39) |
V800G |
possibly damaging |
Het |
Gcm1 |
T |
C |
9: 77,971,844 (GRCm39) |
F262L |
probably benign |
Het |
Gm21983 |
T |
C |
7: 26,879,605 (GRCm39) |
M121V |
probably benign |
Het |
Gm9996 |
A |
T |
10: 29,019,657 (GRCm39) |
|
probably benign |
Het |
Gstm3 |
A |
T |
3: 107,876,074 (GRCm39) |
|
probably benign |
Het |
Gsto2 |
G |
T |
19: 47,863,398 (GRCm39) |
E91D |
probably damaging |
Het |
Hs6st3 |
G |
T |
14: 119,376,492 (GRCm39) |
M222I |
possibly damaging |
Het |
Ighv3-6 |
T |
C |
12: 114,251,850 (GRCm39) |
D90G |
probably damaging |
Het |
Itgb1bp1 |
C |
T |
12: 21,326,854 (GRCm39) |
A40T |
possibly damaging |
Het |
Kcns3 |
C |
T |
12: 11,141,872 (GRCm39) |
E276K |
probably benign |
Het |
Lamc3 |
C |
T |
2: 31,813,034 (GRCm39) |
R1007C |
probably damaging |
Het |
Lnx2 |
A |
T |
5: 146,978,877 (GRCm39) |
M125K |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,812,643 (GRCm39) |
N1018K |
probably benign |
Het |
Mctp2 |
T |
A |
7: 71,895,290 (GRCm39) |
S186C |
probably damaging |
Het |
Or1j20 |
A |
T |
2: 36,759,871 (GRCm39) |
T98S |
probably benign |
Het |
Polg |
T |
C |
7: 79,109,519 (GRCm39) |
T433A |
possibly damaging |
Het |
Rdh13 |
C |
T |
7: 4,438,059 (GRCm39) |
V127M |
probably damaging |
Het |
Rdh16 |
A |
G |
10: 127,649,470 (GRCm39) |
T309A |
probably benign |
Het |
Reep5 |
A |
T |
18: 34,506,312 (GRCm39) |
D21E |
probably benign |
Het |
Rptn |
A |
T |
3: 93,304,227 (GRCm39) |
N520I |
probably benign |
Het |
Rttn |
T |
C |
18: 89,047,122 (GRCm39) |
L928P |
probably damaging |
Het |
Slc44a2 |
A |
G |
9: 21,254,273 (GRCm39) |
I212V |
probably benign |
Het |
Snupn |
A |
G |
9: 56,870,332 (GRCm39) |
T71A |
probably benign |
Het |
Ssu2 |
T |
C |
6: 112,359,353 (GRCm39) |
N89S |
probably benign |
Het |
Thsd7a |
A |
G |
6: 12,321,071 (GRCm39) |
S1535P |
probably damaging |
Het |
Tmt1a |
C |
A |
15: 100,202,933 (GRCm39) |
S51* |
probably null |
Het |
Uba7 |
A |
T |
9: 107,858,715 (GRCm39) |
S849C |
probably benign |
Het |
Vmn2r80 |
A |
G |
10: 79,007,439 (GRCm39) |
T472A |
probably benign |
Het |
Wdr6 |
A |
G |
9: 108,455,743 (GRCm39) |
I17T |
probably benign |
Het |
Xkr9 |
G |
A |
1: 13,771,173 (GRCm39) |
V230I |
probably benign |
Het |
|
Other mutations in Ddias |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02727:Ddias
|
APN |
7 |
92,515,830 (GRCm39) |
missense |
probably damaging |
0.98 |
I0000:Ddias
|
UTSW |
7 |
92,515,848 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0094:Ddias
|
UTSW |
7 |
92,509,108 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0482:Ddias
|
UTSW |
7 |
92,508,736 (GRCm39) |
missense |
probably benign |
0.41 |
R0883:Ddias
|
UTSW |
7 |
92,508,545 (GRCm39) |
missense |
probably benign |
|
R1131:Ddias
|
UTSW |
7 |
92,509,094 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1722:Ddias
|
UTSW |
7 |
92,509,250 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1758:Ddias
|
UTSW |
7 |
92,508,571 (GRCm39) |
missense |
probably benign |
0.03 |
R1937:Ddias
|
UTSW |
7 |
92,507,830 (GRCm39) |
missense |
probably benign |
0.07 |
R2067:Ddias
|
UTSW |
7 |
92,508,907 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2124:Ddias
|
UTSW |
7 |
92,507,464 (GRCm39) |
missense |
probably benign |
0.00 |
R2483:Ddias
|
UTSW |
7 |
92,508,800 (GRCm39) |
missense |
probably benign |
0.13 |
R3623:Ddias
|
UTSW |
7 |
92,508,800 (GRCm39) |
missense |
probably benign |
0.13 |
R3690:Ddias
|
UTSW |
7 |
92,509,366 (GRCm39) |
missense |
probably benign |
0.24 |
R4015:Ddias
|
UTSW |
7 |
92,509,069 (GRCm39) |
missense |
probably benign |
0.06 |
R4021:Ddias
|
UTSW |
7 |
92,510,686 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4022:Ddias
|
UTSW |
7 |
92,510,686 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4384:Ddias
|
UTSW |
7 |
92,507,431 (GRCm39) |
missense |
probably damaging |
0.98 |
R4410:Ddias
|
UTSW |
7 |
92,507,287 (GRCm39) |
missense |
probably benign |
0.04 |
R4691:Ddias
|
UTSW |
7 |
92,508,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R5653:Ddias
|
UTSW |
7 |
92,507,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R6666:Ddias
|
UTSW |
7 |
92,507,289 (GRCm39) |
missense |
probably benign |
|
R6853:Ddias
|
UTSW |
7 |
92,508,773 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7650:Ddias
|
UTSW |
7 |
92,508,143 (GRCm39) |
missense |
probably benign |
0.00 |
R8446:Ddias
|
UTSW |
7 |
92,515,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R8480:Ddias
|
UTSW |
7 |
92,508,608 (GRCm39) |
missense |
probably benign |
0.01 |
R8753:Ddias
|
UTSW |
7 |
92,508,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Ddias
|
UTSW |
7 |
92,507,608 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9336:Ddias
|
UTSW |
7 |
92,507,314 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9554:Ddias
|
UTSW |
7 |
92,507,560 (GRCm39) |
missense |
probably benign |
0.22 |
X0027:Ddias
|
UTSW |
7 |
92,508,203 (GRCm39) |
missense |
probably damaging |
0.99 |
|