Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arap3 |
T |
A |
18: 37,990,560 |
E441V |
probably damaging |
Het |
Arfip2 |
T |
A |
7: 105,637,988 |
D64V |
probably damaging |
Het |
Atg9a |
C |
A |
1: 75,185,685 |
R527L |
probably damaging |
Het |
Atp1a1 |
T |
G |
3: 101,590,548 |
I308L |
probably benign |
Het |
Bcan |
T |
A |
3: 87,996,581 |
Y199F |
probably damaging |
Het |
Bsn |
T |
C |
9: 108,109,992 |
|
probably benign |
Het |
Ccdc158 |
A |
T |
5: 92,632,508 |
L902H |
probably damaging |
Het |
Dnah9 |
G |
T |
11: 66,072,779 |
H1783N |
probably damaging |
Het |
Dpep2 |
A |
G |
8: 105,988,998 |
V320A |
possibly damaging |
Het |
Dsc2 |
A |
G |
18: 20,045,502 |
Y282H |
probably damaging |
Het |
Egfr |
C |
T |
11: 16,911,562 |
P1114S |
probably benign |
Het |
Fastkd1 |
A |
G |
2: 69,700,133 |
S560P |
probably damaging |
Het |
Gm10696 |
T |
G |
3: 94,176,298 |
K69Q |
possibly damaging |
Het |
Gm14295 |
G |
A |
2: 176,811,102 |
R795Q |
possibly damaging |
Het |
Gpr155 |
C |
T |
2: 73,382,127 |
V51I |
probably benign |
Het |
Gsap |
G |
A |
5: 21,222,440 |
|
probably null |
Het |
Hecw1 |
T |
A |
13: 14,377,706 |
I103F |
probably damaging |
Het |
Herc3 |
T |
A |
6: 58,887,437 |
N685K |
probably damaging |
Het |
Hnrnph1 |
T |
A |
11: 50,382,816 |
D244E |
probably benign |
Het |
Hydin |
A |
G |
8: 110,582,049 |
E3989G |
probably benign |
Het |
Ibsp |
T |
C |
5: 104,310,430 |
Y278H |
probably damaging |
Het |
Ift57 |
T |
G |
16: 49,759,340 |
N291K |
probably benign |
Het |
Il15ra |
A |
G |
2: 11,723,571 |
T149A |
possibly damaging |
Het |
Ints5 |
C |
T |
19: 8,896,282 |
T535I |
possibly damaging |
Het |
Jarid2 |
T |
C |
13: 44,902,539 |
L268P |
probably damaging |
Het |
Klhdc7a |
T |
A |
4: 139,965,810 |
T609S |
probably benign |
Het |
Lrrc49 |
A |
G |
9: 60,602,682 |
V429A |
probably benign |
Het |
Lsm3 |
T |
C |
6: 91,522,272 |
V87A |
possibly damaging |
Het |
Man1c1 |
G |
C |
4: 134,703,438 |
P11R |
probably damaging |
Het |
Map1a |
G |
T |
2: 121,307,932 |
V2726L |
probably damaging |
Het |
Marveld3 |
A |
C |
8: 109,961,846 |
S88A |
probably benign |
Het |
Mcm9 |
T |
C |
10: 53,548,574 |
D640G |
probably damaging |
Het |
Mettl4 |
A |
G |
17: 94,733,163 |
I399T |
probably benign |
Het |
Mmp27 |
T |
A |
9: 7,577,378 |
L274* |
probably null |
Het |
Nacc2 |
A |
C |
2: 26,060,223 |
D500E |
probably benign |
Het |
Nprl3 |
T |
A |
11: 32,234,894 |
M372L |
probably benign |
Het |
Olfr478 |
A |
T |
7: 108,031,467 |
I292N |
probably damaging |
Het |
Otud7b |
T |
G |
3: 96,153,520 |
|
probably null |
Het |
Pcx |
G |
A |
19: 4,620,881 |
R1070H |
probably benign |
Het |
Ptprq |
C |
T |
10: 107,590,994 |
W1560* |
probably null |
Het |
Puf60 |
A |
T |
15: 76,070,464 |
I520N |
probably damaging |
Het |
Qars |
C |
T |
9: 108,509,200 |
R143C |
probably damaging |
Het |
Rfx3 |
G |
A |
19: 27,815,494 |
Q322* |
probably null |
Het |
Samd14 |
G |
T |
11: 95,014,391 |
V10L |
probably benign |
Het |
Setd2 |
G |
A |
9: 110,549,844 |
R909Q |
probably benign |
Het |
Sh2d4a |
T |
C |
8: 68,296,664 |
S117P |
probably benign |
Het |
Sharpin |
C |
A |
15: 76,350,666 |
|
probably benign |
Het |
Skor1 |
C |
A |
9: 63,145,122 |
A494S |
possibly damaging |
Het |
Slc41a2 |
T |
C |
10: 83,283,774 |
T375A |
probably benign |
Het |
Sparc |
G |
A |
11: 55,395,801 |
Q324* |
probably null |
Het |
Srebf1 |
T |
C |
11: 60,206,502 |
T171A |
probably benign |
Het |
Srrd |
A |
G |
5: 112,341,122 |
I54T |
possibly damaging |
Het |
Tecpr1 |
G |
T |
5: 144,196,417 |
Q1072K |
probably damaging |
Het |
Tecpr1 |
A |
T |
5: 144,211,456 |
V377E |
probably benign |
Het |
Tln1 |
T |
A |
4: 43,545,721 |
H919L |
probably benign |
Het |
Tm9sf3 |
C |
T |
19: 41,217,420 |
S516N |
probably damaging |
Het |
Trpa1 |
T |
A |
1: 14,881,656 |
T940S |
probably benign |
Het |
Trpv4 |
G |
A |
5: 114,644,710 |
R64C |
probably damaging |
Het |
Tufm |
A |
G |
7: 126,488,847 |
E174G |
probably benign |
Het |
Urb2 |
A |
G |
8: 124,031,102 |
T1183A |
probably damaging |
Het |
Virma |
A |
T |
4: 11,527,843 |
M1245L |
possibly damaging |
Het |
Vmn2r32 |
T |
C |
7: 7,474,615 |
Y259C |
probably damaging |
Het |
Zfp329 |
A |
G |
7: 12,810,767 |
F277L |
probably damaging |
Het |
Zfp683 |
C |
T |
4: 134,055,795 |
T190I |
possibly damaging |
Het |
|