Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930408O17Rik |
G |
A |
12: 104,871,307 |
|
noncoding transcript |
Het |
Adam33 |
G |
A |
2: 131,053,158 |
|
probably benign |
Het |
Akr7a5 |
C |
A |
4: 139,314,269 |
A163D |
probably damaging |
Het |
Arap1 |
T |
C |
7: 101,388,730 |
|
probably benign |
Het |
Arhgap8 |
A |
G |
15: 84,770,035 |
I306V |
possibly damaging |
Het |
Asf1a |
C |
T |
10: 53,606,143 |
A17V |
probably benign |
Het |
Atp1a4 |
A |
T |
1: 172,257,962 |
S25T |
probably benign |
Het |
BC030867 |
C |
T |
11: 102,255,039 |
S47F |
probably damaging |
Het |
Cbln4 |
T |
C |
2: 172,042,208 |
I31V |
probably benign |
Het |
Ccdc93 |
T |
G |
1: 121,448,276 |
L172R |
possibly damaging |
Het |
Ceacam9 |
T |
C |
7: 16,723,619 |
|
probably benign |
Het |
Crhr1 |
C |
A |
11: 104,163,883 |
N107K |
probably benign |
Het |
Cyp11b1 |
T |
A |
15: 74,835,797 |
M488L |
probably benign |
Het |
Dnhd1 |
G |
A |
7: 105,721,744 |
V4744M |
probably damaging |
Het |
Dstyk |
C |
A |
1: 132,449,926 |
N423K |
probably benign |
Het |
Exph5 |
T |
C |
9: 53,375,641 |
S1341P |
probably damaging |
Het |
Fam161b |
T |
C |
12: 84,354,753 |
H409R |
probably benign |
Het |
Fbxo21 |
A |
G |
5: 117,994,668 |
|
probably benign |
Het |
Flt1 |
A |
G |
5: 147,681,741 |
I230T |
probably damaging |
Het |
Gm9931 |
T |
C |
1: 147,281,628 |
|
noncoding transcript |
Het |
Grk6 |
T |
C |
13: 55,449,361 |
F36L |
possibly damaging |
Het |
Grm1 |
G |
T |
10: 10,719,976 |
A636D |
probably damaging |
Het |
Hectd1 |
A |
T |
12: 51,754,133 |
|
probably benign |
Het |
Hltf |
G |
A |
3: 20,092,807 |
V577I |
possibly damaging |
Het |
Lrrc8c |
A |
G |
5: 105,607,493 |
D378G |
probably damaging |
Het |
Mcoln1 |
C |
A |
8: 3,512,657 |
S6* |
probably null |
Het |
Meis1 |
A |
T |
11: 19,011,292 |
S194T |
probably benign |
Het |
Myo1h |
A |
C |
5: 114,353,911 |
|
probably benign |
Het |
Nop9 |
T |
A |
14: 55,753,283 |
C557* |
probably null |
Het |
Nrap |
T |
C |
19: 56,321,000 |
D1619G |
probably damaging |
Het |
Olfr1314 |
A |
T |
2: 112,092,016 |
H228Q |
probably benign |
Het |
Olfr854 |
A |
G |
9: 19,567,198 |
M59T |
probably damaging |
Het |
Olfr934 |
T |
A |
9: 38,982,546 |
Y166F |
possibly damaging |
Het |
Pard3b |
T |
A |
1: 61,767,950 |
D41E |
possibly damaging |
Het |
Parp14 |
G |
T |
16: 35,858,597 |
Q334K |
probably benign |
Het |
Phf3 |
A |
T |
1: 30,808,778 |
I1228K |
probably damaging |
Het |
Polr1b |
T |
A |
2: 129,123,879 |
F814I |
probably benign |
Het |
Rsph1 |
T |
G |
17: 31,258,116 |
S282R |
probably benign |
Het |
Son |
T |
C |
16: 91,656,104 |
S580P |
possibly damaging |
Het |
Sptbn5 |
G |
T |
2: 120,047,617 |
|
probably benign |
Het |
Ssr2 |
T |
A |
3: 88,583,788 |
|
probably null |
Het |
Tfpt |
A |
G |
7: 3,629,040 |
S24P |
probably damaging |
Het |
Tg |
A |
G |
15: 66,705,348 |
T1507A |
probably benign |
Het |
Trpm7 |
A |
G |
2: 126,799,243 |
|
probably benign |
Het |
Wwox |
G |
A |
8: 114,448,159 |
|
probably null |
Het |
Ythdf2 |
C |
T |
4: 132,204,508 |
R447H |
possibly damaging |
Het |
Zfp385c |
A |
G |
11: 100,629,019 |
F368S |
probably damaging |
Het |
Zfp488 |
A |
G |
14: 33,970,400 |
S269P |
possibly damaging |
Het |
Zhx1 |
A |
C |
15: 58,054,049 |
V267G |
possibly damaging |
Het |
|