Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd5 |
T |
A |
9: 122,180,880 (GRCm39) |
V10E |
probably benign |
Het |
Adss2 |
A |
T |
1: 177,601,280 (GRCm39) |
|
probably benign |
Het |
AI467606 |
A |
T |
7: 126,691,673 (GRCm39) |
I83F |
probably damaging |
Het |
Atn1 |
A |
T |
6: 124,723,923 (GRCm39) |
W437R |
unknown |
Het |
Atxn7l2 |
T |
C |
3: 108,116,290 (GRCm39) |
|
probably benign |
Het |
AU040320 |
T |
C |
4: 126,734,936 (GRCm39) |
F750S |
possibly damaging |
Het |
B3gnt6 |
A |
G |
7: 97,842,821 (GRCm39) |
S380P |
probably benign |
Het |
Bod1l |
T |
C |
5: 41,946,215 (GRCm39) |
Q3020R |
probably damaging |
Het |
Borcs6 |
A |
T |
11: 68,950,828 (GRCm39) |
I69F |
probably benign |
Het |
Brd7 |
T |
A |
8: 89,081,340 (GRCm39) |
M170L |
probably benign |
Het |
Ccdc191 |
T |
A |
16: 43,710,581 (GRCm39) |
|
probably benign |
Het |
Cit |
C |
T |
5: 116,064,534 (GRCm39) |
T472I |
possibly damaging |
Het |
Ddx25 |
G |
T |
9: 35,468,685 (GRCm39) |
D57E |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,674,436 (GRCm39) |
L447* |
probably null |
Het |
Epb41l3 |
A |
G |
17: 69,554,641 (GRCm39) |
D247G |
probably damaging |
Het |
Epha8 |
G |
T |
4: 136,665,897 (GRCm39) |
L420M |
probably damaging |
Het |
Etaa1 |
A |
T |
11: 17,890,254 (GRCm39) |
V869E |
probably damaging |
Het |
Exoc8 |
T |
A |
8: 125,622,769 (GRCm39) |
I533F |
probably benign |
Het |
Fam117a |
A |
G |
11: 95,254,823 (GRCm39) |
|
probably null |
Het |
Fam222a |
C |
T |
5: 114,749,092 (GRCm39) |
T96I |
possibly damaging |
Het |
Farsa |
C |
T |
8: 85,594,228 (GRCm39) |
T326I |
probably damaging |
Het |
Fkbp1b |
T |
A |
12: 4,891,401 (GRCm39) |
D12V |
probably damaging |
Het |
Gc |
C |
T |
5: 89,589,421 (GRCm39) |
|
probably null |
Het |
Git2 |
T |
C |
5: 114,868,256 (GRCm39) |
E705G |
probably damaging |
Het |
Gm10318 |
G |
A |
10: 77,689,078 (GRCm39) |
C128Y |
unknown |
Het |
H3c3 |
C |
A |
13: 23,929,393 (GRCm39) |
A30S |
probably benign |
Het |
Hcar2 |
G |
A |
5: 124,002,571 (GRCm39) |
R311* |
probably null |
Het |
Hira |
A |
G |
16: 18,746,261 (GRCm39) |
Q468R |
possibly damaging |
Het |
Hspa1l |
T |
C |
17: 35,197,092 (GRCm39) |
V377A |
probably damaging |
Het |
Igkv2-137 |
T |
A |
6: 67,532,659 (GRCm39) |
W14R |
probably damaging |
Het |
Itga3 |
A |
T |
11: 94,953,391 (GRCm39) |
L317Q |
probably damaging |
Het |
Jade2 |
A |
C |
11: 51,715,906 (GRCm39) |
L433W |
probably damaging |
Het |
Kif21a |
T |
C |
15: 90,840,559 (GRCm39) |
T1186A |
probably benign |
Het |
Krtap28-10 |
C |
A |
1: 83,019,894 (GRCm39) |
C82F |
unknown |
Het |
Ksr1 |
G |
A |
11: 78,931,709 (GRCm39) |
T333M |
probably damaging |
Het |
Msi1 |
T |
C |
5: 115,573,598 (GRCm39) |
F132S |
probably damaging |
Het |
Myo7b |
C |
A |
18: 32,099,402 (GRCm39) |
K1673N |
probably null |
Het |
Myom3 |
T |
A |
4: 135,515,255 (GRCm39) |
N716K |
|
Het |
Ndst4 |
G |
A |
3: 125,515,810 (GRCm39) |
G312R |
probably damaging |
Het |
Ndufaf2 |
A |
G |
13: 108,189,316 (GRCm39) |
V144A |
probably benign |
Het |
Omd |
T |
C |
13: 49,743,576 (GRCm39) |
S209P |
possibly damaging |
Het |
Or2n1c |
A |
G |
17: 38,519,304 (GRCm39) |
H56R |
probably damaging |
Het |
Or2t47 |
G |
C |
11: 58,442,209 (GRCm39) |
N285K |
probably damaging |
Het |
Or51b17 |
G |
A |
7: 103,542,816 (GRCm39) |
T42I |
probably benign |
Het |
Or51e1 |
T |
A |
7: 102,359,219 (GRCm39) |
I251N |
possibly damaging |
Het |
Or52a24 |
T |
C |
7: 103,381,220 (GRCm39) |
I29T |
probably damaging |
Het |
Or52e3 |
T |
C |
7: 102,869,393 (GRCm39) |
L156P |
possibly damaging |
Het |
Patl1 |
T |
A |
19: 11,898,760 (GRCm39) |
Y152N |
probably damaging |
Het |
Plaur |
T |
A |
7: 24,164,577 (GRCm39) |
M27K |
probably benign |
Het |
Ppfia2 |
T |
A |
10: 106,694,439 (GRCm39) |
|
probably benign |
Het |
Ppfia3 |
A |
G |
7: 44,990,100 (GRCm39) |
V1142A |
probably damaging |
Het |
Psg28 |
T |
A |
7: 18,156,981 (GRCm39) |
N418I |
probably damaging |
Het |
Ptprd |
A |
T |
4: 75,863,251 (GRCm39) |
F1237I |
probably damaging |
Het |
Ptprj |
G |
A |
2: 90,270,987 (GRCm39) |
P1247L |
probably damaging |
Het |
Rbms3 |
A |
T |
9: 116,524,886 (GRCm39) |
|
probably null |
Het |
Rgs18 |
A |
G |
1: 144,629,566 (GRCm39) |
V231A |
probably benign |
Het |
Rnf112 |
T |
C |
11: 61,343,277 (GRCm39) |
R156G |
possibly damaging |
Het |
Rsad1 |
A |
C |
11: 94,439,010 (GRCm39) |
V150G |
probably damaging |
Het |
Rxrg |
G |
A |
1: 167,462,005 (GRCm39) |
V350I |
possibly damaging |
Het |
Sash1 |
A |
G |
10: 8,626,808 (GRCm39) |
I192T |
possibly damaging |
Het |
Slc25a36 |
G |
A |
9: 96,961,259 (GRCm39) |
T259I |
probably benign |
Het |
Smarcd3 |
T |
A |
5: 24,798,986 (GRCm39) |
E324V |
probably null |
Het |
St3gal4 |
A |
G |
9: 34,966,944 (GRCm39) |
V2A |
possibly damaging |
Het |
Stk17b |
A |
C |
1: 53,796,784 (GRCm39) |
S328A |
probably benign |
Het |
Tbrg1 |
A |
G |
9: 37,563,949 (GRCm39) |
Y229H |
probably damaging |
Het |
Tdg |
A |
G |
10: 82,484,514 (GRCm39) |
N409S |
probably benign |
Het |
Terb1 |
T |
C |
8: 105,212,036 (GRCm39) |
E315G |
possibly damaging |
Het |
Tmem131 |
A |
G |
1: 36,867,228 (GRCm39) |
F402L |
probably benign |
Het |
Trav4-2 |
T |
C |
14: 53,656,190 (GRCm39) |
I64T |
probably benign |
Het |
Trav4-4-dv10 |
A |
G |
14: 53,921,574 (GRCm39) |
T91A |
probably benign |
Het |
Xdh |
C |
T |
17: 74,228,346 (GRCm39) |
G352R |
probably damaging |
Het |
Zfp551 |
C |
A |
7: 12,156,559 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Garin3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01647:Garin3
|
APN |
11 |
46,296,224 (GRCm39) |
nonsense |
probably null |
|
IGL02375:Garin3
|
APN |
11 |
46,297,379 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02571:Garin3
|
APN |
11 |
46,296,072 (GRCm39) |
missense |
probably damaging |
0.99 |
R0013:Garin3
|
UTSW |
11 |
46,297,631 (GRCm39) |
missense |
unknown |
|
R1902:Garin3
|
UTSW |
11 |
46,297,838 (GRCm39) |
missense |
probably benign |
0.44 |
R1985:Garin3
|
UTSW |
11 |
46,298,693 (GRCm39) |
makesense |
probably null |
|
R2079:Garin3
|
UTSW |
11 |
46,295,934 (GRCm39) |
missense |
probably benign |
0.14 |
R2151:Garin3
|
UTSW |
11 |
46,296,158 (GRCm39) |
nonsense |
probably null |
|
R2857:Garin3
|
UTSW |
11 |
46,296,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R2859:Garin3
|
UTSW |
11 |
46,296,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Garin3
|
UTSW |
11 |
46,295,780 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4232:Garin3
|
UTSW |
11 |
46,298,232 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4342:Garin3
|
UTSW |
11 |
46,298,043 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4679:Garin3
|
UTSW |
11 |
46,295,640 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5119:Garin3
|
UTSW |
11 |
46,297,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R5207:Garin3
|
UTSW |
11 |
46,295,990 (GRCm39) |
missense |
probably benign |
0.13 |
R5540:Garin3
|
UTSW |
11 |
46,295,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R6618:Garin3
|
UTSW |
11 |
46,298,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R6862:Garin3
|
UTSW |
11 |
46,298,418 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7036:Garin3
|
UTSW |
11 |
46,298,235 (GRCm39) |
missense |
|
|
R7489:Garin3
|
UTSW |
11 |
46,298,268 (GRCm39) |
missense |
|
|
R7809:Garin3
|
UTSW |
11 |
46,298,631 (GRCm39) |
missense |
|
|
R7822:Garin3
|
UTSW |
11 |
46,295,730 (GRCm39) |
missense |
|
|
R7996:Garin3
|
UTSW |
11 |
46,295,889 (GRCm39) |
missense |
|
|
R9324:Garin3
|
UTSW |
11 |
46,295,810 (GRCm39) |
missense |
|
|
R9532:Garin3
|
UTSW |
11 |
46,297,673 (GRCm39) |
missense |
|
|
Z1088:Garin3
|
UTSW |
11 |
46,298,550 (GRCm39) |
missense |
possibly damaging |
0.87 |
|