Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030J22Rik |
T |
C |
8: 117,700,376 (GRCm39) |
T9A |
probably benign |
Het |
Abcc5 |
A |
T |
16: 20,215,784 (GRCm39) |
S414R |
possibly damaging |
Het |
Acads |
C |
A |
5: 115,249,057 (GRCm39) |
Q365H |
probably damaging |
Het |
Ankib1 |
G |
T |
5: 3,772,576 (GRCm39) |
Q487K |
probably benign |
Het |
BC034090 |
T |
G |
1: 155,108,229 (GRCm39) |
S11R |
probably damaging |
Het |
Car12 |
A |
G |
9: 66,654,945 (GRCm39) |
N125S |
probably benign |
Het |
Casq1 |
A |
G |
1: 172,044,416 (GRCm39) |
V137A |
probably benign |
Het |
Cfap54 |
C |
A |
10: 92,883,840 (GRCm39) |
V305F |
probably damaging |
Het |
Clstn3 |
T |
C |
6: 124,433,948 (GRCm39) |
E404G |
probably benign |
Het |
Copg1 |
T |
G |
6: 87,870,824 (GRCm39) |
L209R |
probably damaging |
Het |
Cpb2 |
A |
T |
14: 75,493,449 (GRCm39) |
Q42L |
possibly damaging |
Het |
Cpd |
G |
A |
11: 76,693,151 (GRCm39) |
Q712* |
probably null |
Het |
Csmd3 |
T |
A |
15: 47,450,361 (GRCm39) |
Y2690F |
|
Het |
Dchs1 |
G |
T |
7: 105,407,835 (GRCm39) |
T1999K |
probably benign |
Het |
Ddx10 |
T |
A |
9: 53,151,786 (GRCm39) |
T80S |
probably damaging |
Het |
Dmtn |
G |
A |
14: 70,854,768 (GRCm39) |
T69I |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,370,524 (GRCm39) |
H2821Q |
probably damaging |
Het |
Fam162b |
T |
A |
10: 51,466,572 (GRCm39) |
|
probably benign |
Het |
Fam193b |
A |
C |
13: 55,690,612 (GRCm39) |
S717A |
probably benign |
Het |
Far2 |
T |
C |
6: 148,082,493 (GRCm39) |
F500L |
unknown |
Het |
Focad |
T |
A |
4: 88,192,435 (GRCm39) |
V588D |
unknown |
Het |
Gm12728 |
T |
C |
4: 105,651,593 (GRCm39) |
F68L |
probably damaging |
Het |
Gm1527 |
T |
A |
3: 28,974,621 (GRCm39) |
M478K |
probably benign |
Het |
Gm57858 |
T |
A |
3: 36,080,070 (GRCm39) |
D229V |
possibly damaging |
Het |
Gpd2 |
A |
T |
2: 57,230,171 (GRCm39) |
I308F |
probably damaging |
Het |
Igf2bp3 |
T |
C |
6: 49,085,933 (GRCm39) |
T249A |
probably benign |
Het |
Igfn1 |
C |
A |
1: 135,889,746 (GRCm39) |
V2434F |
probably damaging |
Het |
Inhca |
G |
A |
9: 103,156,680 (GRCm39) |
Q127* |
probably null |
Het |
Kdm5a |
C |
A |
6: 120,382,879 (GRCm39) |
Q737K |
probably benign |
Het |
Khdrbs2 |
T |
C |
1: 32,372,685 (GRCm39) |
S120P |
unknown |
Het |
Lmx1a |
T |
C |
1: 167,519,609 (GRCm39) |
F46L |
probably damaging |
Het |
Lrba |
C |
G |
3: 86,232,381 (GRCm39) |
T776R |
probably damaging |
Het |
Lrrc8c |
A |
G |
5: 105,755,701 (GRCm39) |
N492S |
possibly damaging |
Het |
Mapk3 |
A |
T |
7: 126,363,967 (GRCm39) |
I365F |
|
Het |
Mcee |
A |
G |
7: 64,061,657 (GRCm39) |
I153M |
possibly damaging |
Het |
Mllt3 |
T |
C |
4: 87,710,180 (GRCm39) |
D415G |
possibly damaging |
Het |
Muc4 |
A |
T |
16: 32,575,740 (GRCm39) |
T1747S |
unknown |
Het |
Myh14 |
A |
T |
7: 44,310,466 (GRCm39) |
V139E |
probably damaging |
Het |
Myo10 |
A |
T |
15: 25,779,706 (GRCm39) |
I772L |
probably benign |
Het |
Naa15 |
T |
G |
3: 51,367,268 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
T |
A |
1: 60,283,969 (GRCm39) |
I841N |
probably damaging |
Het |
Nf1 |
C |
T |
11: 79,437,102 (GRCm39) |
T2006I |
probably damaging |
Het |
Npr2 |
T |
A |
4: 43,641,254 (GRCm39) |
W427R |
probably damaging |
Het |
Nr1h3 |
A |
T |
2: 91,020,540 (GRCm39) |
F324L |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,947,740 (GRCm39) |
K4430E |
|
Het |
Or1e1d-ps1 |
T |
A |
11: 73,819,013 (GRCm39) |
Y61N |
possibly damaging |
Het |
Or5ac21 |
A |
G |
16: 59,124,391 (GRCm39) |
R292G |
probably damaging |
Het |
Or6c2 |
A |
T |
10: 129,362,530 (GRCm39) |
T145S |
probably benign |
Het |
Or6d13 |
T |
C |
6: 116,517,894 (GRCm39) |
L160P |
probably benign |
Het |
Osgin1 |
T |
A |
8: 120,172,170 (GRCm39) |
H321Q |
probably benign |
Het |
P4ha1 |
A |
G |
10: 59,186,273 (GRCm39) |
I251V |
probably benign |
Het |
Padi2 |
G |
A |
4: 140,644,997 (GRCm39) |
W77* |
probably null |
Het |
Pkd1 |
T |
A |
17: 24,800,616 (GRCm39) |
I3086N |
probably damaging |
Het |
Plk3 |
T |
C |
4: 116,988,350 (GRCm39) |
N360S |
probably benign |
Het |
Prr14 |
A |
T |
7: 127,075,614 (GRCm39) |
S541C |
probably null |
Het |
Ptch2 |
C |
A |
4: 116,971,843 (GRCm39) |
Q1122K |
possibly damaging |
Het |
Rab3gap1 |
T |
C |
1: 127,865,727 (GRCm39) |
V764A |
possibly damaging |
Het |
Rad50 |
T |
C |
11: 53,586,223 (GRCm39) |
I258V |
probably benign |
Het |
Rapgef3 |
G |
T |
15: 97,664,672 (GRCm39) |
R64S |
probably benign |
Het |
Rbm44 |
A |
G |
1: 91,079,938 (GRCm39) |
N42S |
possibly damaging |
Het |
Ring1 |
T |
C |
17: 34,240,694 (GRCm39) |
Y361C |
probably damaging |
Het |
Robo3 |
T |
C |
9: 37,329,852 (GRCm39) |
T1155A |
probably damaging |
Het |
Rsf1 |
GGCGG |
GGCGGTGGCCGCGG |
7: 97,229,122 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,470,502 (GRCm39) |
T4682A |
probably damaging |
Het |
Scart1 |
A |
T |
7: 139,804,790 (GRCm39) |
N598Y |
possibly damaging |
Het |
Sema7a |
T |
C |
9: 57,868,847 (GRCm39) |
V653A |
unknown |
Het |
Slc16a13 |
T |
C |
11: 70,110,105 (GRCm39) |
Y132C |
probably damaging |
Het |
Slc24a1 |
A |
G |
9: 64,855,815 (GRCm39) |
V364A |
unknown |
Het |
Slc8a2 |
C |
T |
7: 15,868,278 (GRCm39) |
A170V |
probably damaging |
Het |
Snx2 |
T |
C |
18: 53,327,640 (GRCm39) |
V122A |
probably benign |
Het |
Sstr1 |
A |
T |
12: 58,260,066 (GRCm39) |
M230L |
probably benign |
Het |
Themis2 |
C |
T |
4: 132,513,528 (GRCm39) |
V233I |
possibly damaging |
Het |
Tmem106b |
T |
C |
6: 13,078,167 (GRCm39) |
S121P |
probably damaging |
Het |
Tmem63c |
A |
G |
12: 87,124,722 (GRCm39) |
I529V |
probably benign |
Het |
Tmem94 |
T |
C |
11: 115,686,971 (GRCm39) |
|
probably null |
Het |
Trmt10c |
A |
T |
16: 55,854,619 (GRCm39) |
W339R |
probably damaging |
Het |
Ugt2b1 |
A |
T |
5: 87,065,578 (GRCm39) |
F487Y |
not run |
Het |
Vmn2r91 |
T |
A |
17: 18,356,838 (GRCm39) |
L835* |
probably null |
Het |
Vps52 |
C |
A |
17: 34,177,283 (GRCm39) |
N108K |
possibly damaging |
Het |
Wdpcp |
T |
A |
11: 21,661,585 (GRCm39) |
C286S |
possibly damaging |
Het |
Zfp959 |
T |
A |
17: 56,205,551 (GRCm39) |
H529Q |
possibly damaging |
Het |
|
Other mutations in Slfn8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00500:Slfn8
|
APN |
11 |
82,904,310 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01418:Slfn8
|
APN |
11 |
82,895,462 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01620:Slfn8
|
APN |
11 |
82,895,059 (GRCm39) |
nonsense |
probably null |
|
IGL01875:Slfn8
|
APN |
11 |
82,894,905 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01896:Slfn8
|
APN |
11 |
82,894,522 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01929:Slfn8
|
APN |
11 |
82,894,231 (GRCm39) |
nonsense |
probably null |
|
IGL02111:Slfn8
|
APN |
11 |
82,895,324 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02136:Slfn8
|
APN |
11 |
82,894,291 (GRCm39) |
nonsense |
probably null |
|
IGL02165:Slfn8
|
APN |
11 |
82,908,022 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02645:Slfn8
|
APN |
11 |
82,894,380 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02682:Slfn8
|
APN |
11 |
82,894,517 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02689:Slfn8
|
APN |
11 |
82,907,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02948:Slfn8
|
APN |
11 |
82,894,078 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03037:Slfn8
|
APN |
11 |
82,894,078 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03185:Slfn8
|
APN |
11 |
82,908,333 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03243:Slfn8
|
APN |
11 |
82,894,533 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03286:Slfn8
|
APN |
11 |
82,904,294 (GRCm39) |
missense |
probably damaging |
0.99 |
seven_dwarfs
|
UTSW |
11 |
82,894,160 (GRCm39) |
missense |
probably benign |
0.09 |
vanwinkle
|
UTSW |
11 |
82,908,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Slfn8
|
UTSW |
11 |
82,894,169 (GRCm39) |
nonsense |
probably null |
|
R0368:Slfn8
|
UTSW |
11 |
82,907,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R0382:Slfn8
|
UTSW |
11 |
82,895,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R0655:Slfn8
|
UTSW |
11 |
82,894,647 (GRCm39) |
missense |
probably benign |
0.35 |
R0894:Slfn8
|
UTSW |
11 |
82,894,407 (GRCm39) |
missense |
probably benign |
0.07 |
R1006:Slfn8
|
UTSW |
11 |
82,894,337 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1181:Slfn8
|
UTSW |
11 |
82,907,571 (GRCm39) |
missense |
probably benign |
0.19 |
R1187:Slfn8
|
UTSW |
11 |
82,894,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R1501:Slfn8
|
UTSW |
11 |
82,894,006 (GRCm39) |
missense |
probably damaging |
0.99 |
R1646:Slfn8
|
UTSW |
11 |
82,907,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Slfn8
|
UTSW |
11 |
82,894,447 (GRCm39) |
nonsense |
probably null |
|
R2005:Slfn8
|
UTSW |
11 |
82,894,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R2363:Slfn8
|
UTSW |
11 |
82,894,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R3780:Slfn8
|
UTSW |
11 |
82,908,280 (GRCm39) |
missense |
probably benign |
0.13 |
R3890:Slfn8
|
UTSW |
11 |
82,895,270 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3917:Slfn8
|
UTSW |
11 |
82,907,819 (GRCm39) |
nonsense |
probably null |
|
R4559:Slfn8
|
UTSW |
11 |
82,895,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:Slfn8
|
UTSW |
11 |
82,908,332 (GRCm39) |
missense |
probably benign |
0.10 |
R4767:Slfn8
|
UTSW |
11 |
82,894,023 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4773:Slfn8
|
UTSW |
11 |
82,908,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R4859:Slfn8
|
UTSW |
11 |
82,908,540 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R4916:Slfn8
|
UTSW |
11 |
82,907,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R4939:Slfn8
|
UTSW |
11 |
82,894,111 (GRCm39) |
missense |
probably benign |
0.01 |
R5107:Slfn8
|
UTSW |
11 |
82,907,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R5130:Slfn8
|
UTSW |
11 |
82,894,647 (GRCm39) |
missense |
probably benign |
0.35 |
R5165:Slfn8
|
UTSW |
11 |
82,907,953 (GRCm39) |
missense |
probably damaging |
0.99 |
R5238:Slfn8
|
UTSW |
11 |
82,904,214 (GRCm39) |
missense |
probably damaging |
0.96 |
R5282:Slfn8
|
UTSW |
11 |
82,908,550 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5311:Slfn8
|
UTSW |
11 |
82,894,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R5499:Slfn8
|
UTSW |
11 |
82,895,042 (GRCm39) |
missense |
probably damaging |
0.99 |
R5617:Slfn8
|
UTSW |
11 |
82,895,547 (GRCm39) |
missense |
probably benign |
0.01 |
R5782:Slfn8
|
UTSW |
11 |
82,907,867 (GRCm39) |
missense |
probably damaging |
0.98 |
R5823:Slfn8
|
UTSW |
11 |
82,907,562 (GRCm39) |
missense |
probably benign |
0.01 |
R5886:Slfn8
|
UTSW |
11 |
82,894,160 (GRCm39) |
missense |
probably benign |
0.09 |
R5933:Slfn8
|
UTSW |
11 |
82,894,161 (GRCm39) |
missense |
probably benign |
0.00 |
R6151:Slfn8
|
UTSW |
11 |
82,908,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Slfn8
|
UTSW |
11 |
82,894,690 (GRCm39) |
makesense |
probably null |
|
R6191:Slfn8
|
UTSW |
11 |
82,907,626 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6419:Slfn8
|
UTSW |
11 |
82,894,881 (GRCm39) |
splice site |
probably null |
|
R6925:Slfn8
|
UTSW |
11 |
82,904,243 (GRCm39) |
nonsense |
probably null |
|
R7065:Slfn8
|
UTSW |
11 |
82,907,794 (GRCm39) |
missense |
probably benign |
0.01 |
R7414:Slfn8
|
UTSW |
11 |
82,907,618 (GRCm39) |
nonsense |
probably null |
|
R7819:Slfn8
|
UTSW |
11 |
82,895,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R8425:Slfn8
|
UTSW |
11 |
82,895,441 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8517:Slfn8
|
UTSW |
11 |
82,894,968 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8804:Slfn8
|
UTSW |
11 |
82,907,639 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8814:Slfn8
|
UTSW |
11 |
82,907,505 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9069:Slfn8
|
UTSW |
11 |
82,907,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Slfn8
|
UTSW |
11 |
82,894,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R9457:Slfn8
|
UTSW |
11 |
82,908,532 (GRCm39) |
missense |
probably benign |
|
R9678:Slfn8
|
UTSW |
11 |
82,907,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R9708:Slfn8
|
UTSW |
11 |
82,894,267 (GRCm39) |
missense |
probably benign |
0.00 |
R9764:Slfn8
|
UTSW |
11 |
82,907,838 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Slfn8
|
UTSW |
11 |
82,907,754 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1177:Slfn8
|
UTSW |
11 |
82,894,359 (GRCm39) |
missense |
probably benign |
0.11 |
|