Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26b |
G |
A |
8: 43,520,795 |
T390I |
probably benign |
Het |
Adgb |
A |
G |
10: 10,411,712 |
|
probably null |
Het |
Ado |
G |
T |
10: 67,548,435 |
Y113* |
probably null |
Het |
Angptl1 |
A |
G |
1: 156,845,315 |
E237G |
probably damaging |
Het |
Arid2 |
T |
A |
15: 96,356,697 |
Y141* |
probably null |
Het |
Clvs1 |
T |
C |
4: 9,350,739 |
I183T |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,292,338 |
K1817E |
probably benign |
Het |
Eif3e |
C |
A |
15: 43,263,246 |
R271L |
probably damaging |
Het |
Eml6 |
A |
G |
11: 29,753,085 |
V1611A |
probably damaging |
Het |
Enpp3 |
G |
T |
10: 24,784,841 |
Y634* |
probably null |
Het |
Evi5l |
C |
T |
8: 4,200,886 |
R394W |
probably damaging |
Het |
Fcgr3 |
A |
C |
1: 171,054,092 |
F156V |
probably damaging |
Het |
Fmo1 |
T |
A |
1: 162,833,833 |
T294S |
probably benign |
Het |
Gabrb3 |
A |
G |
7: 57,816,455 |
Q339R |
probably damaging |
Het |
Gen1 |
T |
A |
12: 11,242,166 |
T606S |
probably benign |
Het |
Gfod1 |
T |
C |
13: 43,201,052 |
Q149R |
probably benign |
Het |
Golm1 |
A |
G |
13: 59,640,257 |
V276A |
probably benign |
Het |
Hc |
C |
A |
2: 35,024,149 |
V849F |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,321,564 |
I832T |
possibly damaging |
Het |
Hspa14 |
T |
C |
2: 3,496,606 |
D283G |
probably damaging |
Het |
Lztfl1 |
C |
T |
9: 123,712,471 |
W94* |
probably null |
Het |
Lzts3 |
T |
C |
2: 130,635,386 |
S381G |
probably benign |
Het |
Mgat2 |
A |
G |
12: 69,184,670 |
Y6C |
probably damaging |
Het |
Mrpl30 |
T |
C |
1: 37,895,358 |
I27T |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,853,229 |
T1045S |
unknown |
Het |
Nlrp4a |
G |
A |
7: 26,449,265 |
R99Q |
probably benign |
Het |
Olfr1450 |
A |
G |
19: 12,953,642 |
T18A |
possibly damaging |
Het |
Olfr1510 |
T |
C |
14: 52,410,488 |
Y128C |
probably damaging |
Het |
Phlpp1 |
T |
C |
1: 106,281,402 |
L495P |
probably damaging |
Het |
Pla2g4d |
T |
C |
2: 120,279,295 |
D178G |
possibly damaging |
Het |
Prl5a1 |
C |
G |
13: 28,150,014 |
L167V |
probably damaging |
Het |
Sardh |
A |
G |
2: 27,197,639 |
V740A |
probably benign |
Het |
Sbno1 |
T |
G |
5: 124,405,646 |
T277P |
probably benign |
Het |
Slc2a1 |
T |
C |
4: 119,136,265 |
V433A |
probably damaging |
Het |
Slc4a10 |
T |
C |
2: 62,303,964 |
V1008A |
possibly damaging |
Het |
Smarcal1 |
T |
G |
1: 72,586,020 |
S109A |
probably benign |
Het |
Speg |
A |
G |
1: 75,401,190 |
D864G |
probably benign |
Het |
Steap4 |
T |
C |
5: 7,976,976 |
I313T |
probably benign |
Het |
Tab2 |
A |
T |
10: 7,911,105 |
D614E |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,895,403 |
K2246E |
probably damaging |
Het |
Timm23 |
A |
G |
14: 32,180,563 |
S208P |
probably damaging |
Het |
Tmem229a |
C |
A |
6: 24,955,212 |
C181F |
probably benign |
Het |
Ugdh |
T |
C |
5: 65,417,615 |
Y356C |
probably damaging |
Het |
Ugt2a1 |
A |
G |
5: 87,486,727 |
L7P |
probably damaging |
Het |
Uhrf1 |
A |
G |
17: 56,312,905 |
D272G |
possibly damaging |
Het |
Vmn1r206 |
T |
A |
13: 22,620,657 |
I127F |
probably damaging |
Het |
Vmn2r106 |
T |
C |
17: 20,285,228 |
Y68C |
possibly damaging |
Het |
|