Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
C |
A |
11: 58,425,756 |
D187E |
probably damaging |
Het |
9530053A07Rik |
A |
G |
7: 28,144,408 |
N907S |
probably benign |
Het |
A830010M20Rik |
G |
T |
5: 107,507,196 |
V954L |
probably benign |
Het |
A830010M20Rik |
A |
G |
5: 107,510,505 |
D1647G |
probably damaging |
Het |
Abl2 |
T |
C |
1: 156,630,060 |
Y299H |
probably damaging |
Het |
Acsl3 |
T |
A |
1: 78,681,992 |
N120K |
probably damaging |
Het |
Aldh1a1 |
A |
G |
19: 20,629,070 |
K255R |
possibly damaging |
Het |
Baz2b |
C |
T |
2: 59,920,437 |
R1205H |
probably benign |
Het |
Carmil1 |
A |
G |
13: 24,013,404 |
S1350P |
probably benign |
Het |
Cecr2 |
A |
T |
6: 120,761,621 |
N325I |
|
Het |
Cep120 |
C |
T |
18: 53,740,089 |
A57T |
probably damaging |
Het |
Chst8 |
T |
C |
7: 34,748,203 |
|
probably null |
Het |
Cntn4 |
A |
T |
6: 106,525,460 |
I393F |
probably damaging |
Het |
Crocc |
T |
C |
4: 141,022,341 |
D1494G |
probably damaging |
Het |
Cwc25 |
T |
C |
11: 97,748,006 |
E364G |
possibly damaging |
Het |
Drg2 |
A |
G |
11: 60,454,693 |
E5G |
probably benign |
Het |
Ehd4 |
T |
C |
2: 120,091,248 |
H509R |
probably damaging |
Het |
Enam |
A |
T |
5: 88,502,327 |
N565I |
probably damaging |
Het |
Evi2a |
G |
T |
11: 79,527,423 |
N120K |
probably benign |
Het |
Faim |
A |
G |
9: 98,992,126 |
T2A |
probably benign |
Het |
Fmnl1 |
T |
C |
11: 103,196,265 |
V836A |
unknown |
Het |
Fosb |
T |
C |
7: 19,305,188 |
I224V |
possibly damaging |
Het |
Frem3 |
A |
T |
8: 80,612,031 |
T318S |
probably damaging |
Het |
Gm13103 |
A |
G |
4: 143,851,881 |
N237S |
possibly damaging |
Het |
Gm9972 |
G |
A |
11: 43,036,804 |
G93R |
unknown |
Het |
Gtf2a1 |
A |
T |
12: 91,567,835 |
I215N |
possibly damaging |
Het |
Hs3st3b1 |
A |
G |
11: 63,921,571 |
V106A |
probably benign |
Het |
Igkv19-93 |
T |
C |
6: 68,736,501 |
D48G |
probably benign |
Het |
Itgb8 |
A |
T |
12: 119,237,708 |
W31R |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,854,104 |
W1995R |
unknown |
Het |
Lama3 |
G |
T |
18: 12,439,392 |
Q551H |
probably damaging |
Het |
Lama5 |
T |
C |
2: 180,201,795 |
Y453C |
probably damaging |
Het |
Lbhd2 |
G |
A |
12: 111,410,290 |
R57H |
probably damaging |
Het |
Lcmt2 |
A |
G |
2: 121,138,790 |
V384A |
probably damaging |
Het |
Lgsn |
T |
G |
1: 31,203,371 |
L178R |
probably damaging |
Het |
Lhcgr |
C |
T |
17: 88,758,383 |
V193I |
probably benign |
Het |
Lta4h |
T |
C |
10: 93,453,511 |
M1T |
probably null |
Het |
Ly6l |
T |
C |
15: 75,449,496 |
S14P |
probably damaging |
Het |
Met |
C |
A |
6: 17,547,012 |
C881* |
probably null |
Het |
Mettl21e |
A |
T |
1: 44,210,239 |
Y86N |
probably damaging |
Het |
Mgam |
A |
T |
6: 40,656,512 |
N251Y |
possibly damaging |
Het |
Mgam |
A |
G |
6: 40,763,111 |
T1673A |
probably benign |
Het |
Mmp27 |
T |
A |
9: 7,578,230 |
V357D |
probably damaging |
Het |
Muc2 |
A |
G |
7: 141,752,744 |
E740G |
|
Het |
Myoc |
C |
A |
1: 162,648,844 |
S372R |
probably benign |
Het |
Ncor2 |
A |
T |
5: 125,020,040 |
M1358K |
|
Het |
Nol6 |
A |
G |
4: 41,119,468 |
S613P |
probably benign |
Het |
Nuggc |
T |
A |
14: 65,617,623 |
I334N |
probably damaging |
Het |
Nxnl2 |
C |
T |
13: 51,171,506 |
P62S |
probably damaging |
Het |
Ogfod1 |
C |
T |
8: 94,037,439 |
H51Y |
possibly damaging |
Het |
Olfml1 |
T |
A |
7: 107,590,323 |
D198E |
possibly damaging |
Het |
Olfr1395 |
A |
C |
11: 49,149,118 |
N287T |
probably damaging |
Het |
Ovch2 |
C |
T |
7: 107,794,370 |
R183H |
possibly damaging |
Het |
Plxnd1 |
A |
T |
6: 115,960,837 |
L1516Q |
probably damaging |
Het |
Prrc2c |
A |
G |
1: 162,679,974 |
V2448A |
possibly damaging |
Het |
Rexo5 |
C |
T |
7: 119,818,413 |
T212I |
probably damaging |
Het |
Rgl2 |
C |
T |
17: 33,933,429 |
R367W |
probably damaging |
Het |
Rnf213 |
T |
G |
11: 119,437,992 |
I2030S |
|
Het |
Rtf1 |
C |
T |
2: 119,675,099 |
A11V |
unknown |
Het |
Setdb1 |
T |
G |
3: 95,338,674 |
T647P |
probably damaging |
Het |
Shisa6 |
G |
C |
11: 66,502,654 |
P272R |
possibly damaging |
Het |
Slc25a54 |
G |
T |
3: 109,116,501 |
G471* |
probably null |
Het |
Slc30a1 |
A |
G |
1: 191,909,432 |
T397A |
probably benign |
Het |
Slc7a14 |
A |
G |
3: 31,227,153 |
F336S |
possibly damaging |
Het |
Slitrk3 |
C |
T |
3: 73,050,465 |
V325I |
possibly damaging |
Het |
Sptan1 |
A |
G |
2: 29,986,929 |
Y361C |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,698,503 |
D1747G |
probably benign |
Het |
Taf3 |
T |
C |
2: 9,951,442 |
E638G |
probably damaging |
Het |
Tbc1d8 |
T |
C |
1: 39,372,533 |
D1074G |
probably benign |
Het |
Tecrl |
G |
A |
5: 83,354,907 |
H32Y |
probably benign |
Het |
Tgm3 |
T |
A |
2: 130,024,561 |
M133K |
probably benign |
Het |
Tmem131 |
A |
G |
1: 36,841,604 |
F195S |
probably damaging |
Het |
Tmem82 |
T |
C |
4: 141,614,950 |
I314V |
possibly damaging |
Het |
Trappc10 |
T |
C |
10: 78,207,493 |
E555G |
probably damaging |
Het |
Ubn2 |
A |
T |
6: 38,452,876 |
K176* |
probably null |
Het |
Ucp1 |
G |
A |
8: 83,293,902 |
G114R |
probably benign |
Het |
Unc5c |
A |
G |
3: 141,677,990 |
D43G |
probably damaging |
Het |
Vmn2r3 |
C |
T |
3: 64,261,404 |
V571M |
possibly damaging |
Het |
Vwa3a |
A |
T |
7: 120,786,465 |
I677L |
probably benign |
Het |
Wdr48 |
T |
C |
9: 119,911,081 |
S319P |
probably damaging |
Het |
|