Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930533K18Rik |
T |
C |
10: 70,708,086 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl2fm1 |
C |
A |
3: 59,840,001 (GRCm39) |
Y24* |
probably null |
Het |
Abl1 |
T |
A |
2: 31,690,656 (GRCm39) |
M706K |
probably benign |
Het |
Abtb1 |
T |
C |
6: 88,813,536 (GRCm39) |
T401A |
probably benign |
Het |
Acd |
A |
G |
8: 106,427,122 (GRCm39) |
L96P |
probably damaging |
Het |
Arsi |
T |
A |
18: 61,045,369 (GRCm39) |
W20R |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Asic3 |
C |
T |
5: 24,618,749 (GRCm39) |
Q14* |
probably null |
Het |
Asxl3 |
T |
A |
18: 22,655,125 (GRCm39) |
I1045N |
probably damaging |
Het |
Atr |
T |
C |
9: 95,818,474 (GRCm39) |
I2149T |
probably damaging |
Het |
Begain |
A |
G |
12: 108,999,025 (GRCm39) |
|
probably null |
Het |
Brca2 |
C |
T |
5: 150,460,387 (GRCm39) |
T554I |
possibly damaging |
Het |
Brd10 |
T |
C |
19: 29,693,814 (GRCm39) |
N1960S |
probably damaging |
Het |
C1s2 |
C |
T |
6: 124,612,641 (GRCm39) |
V11I |
probably benign |
Het |
Cacna1i |
T |
C |
15: 80,260,990 (GRCm39) |
F1333L |
possibly damaging |
Het |
Camsap2 |
T |
C |
1: 136,201,521 (GRCm39) |
T662A |
possibly damaging |
Het |
Cep164 |
C |
T |
9: 45,690,226 (GRCm39) |
V1367M |
probably damaging |
Het |
Cfap46 |
C |
A |
7: 139,219,518 (GRCm39) |
A1316S |
probably benign |
Het |
Cic |
T |
C |
7: 24,987,691 (GRCm39) |
S553P |
probably damaging |
Het |
Cilk1 |
T |
A |
9: 78,065,144 (GRCm39) |
D351E |
probably benign |
Het |
Clcn2 |
C |
T |
16: 20,534,712 (GRCm39) |
A12T |
probably benign |
Het |
Clip2 |
A |
G |
5: 134,532,081 (GRCm39) |
Y540H |
probably benign |
Het |
Coil |
A |
G |
11: 88,872,923 (GRCm39) |
N428S |
possibly damaging |
Het |
Cpxm1 |
A |
C |
2: 130,237,617 (GRCm39) |
V196G |
probably damaging |
Het |
Cr2 |
A |
G |
1: 194,839,624 (GRCm39) |
V601A |
probably damaging |
Het |
Cyp3a25 |
T |
A |
5: 145,921,763 (GRCm39) |
K390N |
probably damaging |
Het |
Dclre1a |
T |
C |
19: 56,535,150 (GRCm39) |
|
probably null |
Het |
Dennd4a |
G |
C |
9: 64,766,640 (GRCm39) |
|
probably null |
Het |
Dlg5 |
T |
C |
14: 24,199,512 (GRCm39) |
H1464R |
probably benign |
Het |
Dmac2 |
T |
G |
7: 25,324,217 (GRCm39) |
M225R |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 30,950,154 (GRCm39) |
V1991A |
possibly damaging |
Het |
Dscam |
A |
C |
16: 96,626,781 (GRCm39) |
V376G |
probably benign |
Het |
Dync1li1 |
A |
G |
9: 114,538,252 (GRCm39) |
D203G |
probably benign |
Het |
Eva1c |
A |
G |
16: 90,663,331 (GRCm39) |
T22A |
probably benign |
Het |
Fam110b |
A |
G |
4: 5,799,029 (GRCm39) |
D149G |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,918,547 (GRCm39) |
I3528F |
probably damaging |
Het |
Fsip1 |
T |
C |
2: 118,063,389 (GRCm39) |
D360G |
probably damaging |
Het |
Galnt14 |
T |
C |
17: 74,016,934 (GRCm39) |
T41A |
probably benign |
Het |
Gdf3 |
T |
A |
6: 122,586,921 (GRCm39) |
Q2L |
probably benign |
Het |
Glrp1 |
A |
G |
1: 88,437,511 (GRCm39) |
|
probably null |
Het |
Gm3336 |
C |
G |
8: 71,173,066 (GRCm39) |
|
probably null |
Het |
Gm8674 |
C |
T |
13: 50,054,844 (GRCm39) |
|
noncoding transcript |
Het |
Gnat1 |
A |
G |
9: 107,553,774 (GRCm39) |
Y226H |
probably damaging |
Het |
Grk5 |
T |
C |
19: 61,078,410 (GRCm39) |
V489A |
probably damaging |
Het |
H1f8 |
A |
G |
6: 115,925,719 (GRCm39) |
Y1C |
probably null |
Het |
Igfbpl1 |
C |
A |
4: 45,826,406 (GRCm39) |
A130S |
probably benign |
Het |
Impdh1 |
T |
A |
6: 29,205,087 (GRCm39) |
D261V |
probably benign |
Het |
Itgal |
T |
A |
7: 126,913,232 (GRCm39) |
S610T |
probably damaging |
Het |
Jcad |
A |
G |
18: 4,649,293 (GRCm39) |
T55A |
probably benign |
Het |
Jup |
G |
A |
11: 100,264,963 (GRCm39) |
R663* |
probably null |
Het |
Kalrn |
C |
T |
16: 34,114,585 (GRCm39) |
G556D |
probably damaging |
Het |
Krt81 |
T |
C |
15: 101,358,020 (GRCm39) |
E411G |
probably damaging |
Het |
Lcat |
T |
C |
8: 106,666,520 (GRCm39) |
E334G |
probably damaging |
Het |
Lhcgr |
T |
C |
17: 89,057,585 (GRCm39) |
E302G |
probably benign |
Het |
Magi1 |
A |
G |
6: 93,676,620 (GRCm39) |
V913A |
possibly damaging |
Het |
Mrpl19 |
A |
T |
6: 81,941,060 (GRCm39) |
|
probably null |
Het |
Muc4 |
G |
T |
16: 32,576,307 (GRCm39) |
|
probably benign |
Het |
Mycbp2 |
A |
G |
14: 103,489,945 (GRCm39) |
V953A |
possibly damaging |
Het |
Myo3a |
G |
A |
2: 22,401,054 (GRCm39) |
V600I |
probably benign |
Het |
Ndufv3 |
G |
A |
17: 31,750,219 (GRCm39) |
R467Q |
probably damaging |
Het |
Ngef |
A |
G |
1: 87,430,986 (GRCm39) |
|
probably null |
Het |
Nisch |
A |
T |
14: 30,898,389 (GRCm39) |
|
probably benign |
Het |
Nlrp4c |
G |
A |
7: 6,069,955 (GRCm39) |
|
probably null |
Het |
Nup153 |
A |
T |
13: 46,867,223 (GRCm39) |
S154T |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,885,658 (GRCm39) |
|
probably benign |
Het |
Or2t1 |
T |
A |
14: 14,328,774 (GRCm38) |
L221Q |
probably damaging |
Het |
Or4a74 |
G |
T |
2: 89,439,693 (GRCm39) |
P251H |
probably damaging |
Het |
Or6c219 |
T |
C |
10: 129,781,206 (GRCm39) |
M242V |
possibly damaging |
Het |
Otogl |
T |
C |
10: 107,615,692 (GRCm39) |
N1869S |
probably benign |
Het |
Phf24 |
G |
T |
4: 42,934,661 (GRCm39) |
C136F |
probably damaging |
Het |
Phldb2 |
A |
T |
16: 45,646,374 (GRCm39) |
V65E |
probably benign |
Het |
Pkhd1 |
C |
A |
1: 20,417,681 (GRCm39) |
G2490V |
probably damaging |
Het |
Prl8a8 |
A |
T |
13: 27,692,433 (GRCm39) |
M186K |
probably damaging |
Het |
Qars1 |
T |
C |
9: 108,391,809 (GRCm39) |
V70A |
probably damaging |
Het |
Rac1 |
C |
T |
5: 143,502,980 (GRCm39) |
V14I |
probably benign |
Het |
Rapgef5 |
T |
A |
12: 117,652,419 (GRCm39) |
|
probably null |
Het |
Slc17a6 |
A |
G |
7: 51,311,294 (GRCm39) |
Y336C |
probably damaging |
Het |
Slc30a9 |
T |
C |
5: 67,505,395 (GRCm39) |
L441P |
probably damaging |
Het |
Slc45a2 |
T |
C |
15: 11,022,172 (GRCm39) |
S305P |
probably damaging |
Het |
Sod3 |
G |
T |
5: 52,525,504 (GRCm39) |
V68L |
probably benign |
Het |
Sp1 |
T |
G |
15: 102,339,438 (GRCm39) |
S773A |
possibly damaging |
Het |
Spen |
C |
A |
4: 141,200,096 (GRCm39) |
G2821C |
probably damaging |
Het |
Tagap1 |
A |
G |
17: 7,223,425 (GRCm39) |
S424P |
probably benign |
Het |
Tbc1d22a |
T |
C |
15: 86,119,770 (GRCm39) |
V22A |
possibly damaging |
Het |
Tfec |
C |
T |
6: 16,840,467 (GRCm39) |
|
probably null |
Het |
Thsd7a |
A |
T |
6: 12,409,041 (GRCm39) |
|
probably null |
Het |
Tnfsf15 |
C |
A |
4: 63,651,588 (GRCm39) |
G112V |
probably benign |
Het |
Tnfsf9 |
A |
G |
17: 57,412,738 (GRCm39) |
T103A |
probably benign |
Het |
Tnxb |
C |
T |
17: 34,911,307 (GRCm39) |
R1537* |
probably null |
Het |
Tpra1 |
A |
G |
6: 88,888,805 (GRCm39) |
N329S |
probably benign |
Het |
Ttc12 |
A |
G |
9: 49,368,184 (GRCm39) |
F281S |
probably damaging |
Het |
Unc79 |
A |
G |
12: 103,025,579 (GRCm39) |
N322S |
probably damaging |
Het |
Unk |
G |
T |
11: 115,921,268 (GRCm39) |
|
probably benign |
Het |
Usp4 |
G |
T |
9: 108,225,207 (GRCm39) |
G31W |
probably damaging |
Het |
Vcan |
G |
T |
13: 89,853,331 (GRCm39) |
A543D |
possibly damaging |
Het |
Vil1 |
A |
C |
1: 74,457,606 (GRCm39) |
I80L |
probably benign |
Het |
Vmn2r27 |
C |
T |
6: 124,208,593 (GRCm39) |
G51S |
probably benign |
Het |
Vpreb1a |
A |
G |
16: 16,686,935 (GRCm39) |
|
probably null |
Het |
Zbtb6 |
C |
T |
2: 37,319,829 (GRCm39) |
C33Y |
probably damaging |
Het |
Zfp330 |
A |
T |
8: 83,492,644 (GRCm39) |
C189* |
probably null |
Het |
Zfp942 |
T |
A |
17: 22,147,522 (GRCm39) |
H369L |
probably damaging |
Het |
Zfp943 |
T |
A |
17: 22,211,361 (GRCm39) |
I149K |
probably benign |
Het |
Zfyve19 |
G |
A |
2: 119,042,016 (GRCm39) |
V162M |
probably benign |
Het |
|
Other mutations in Slc16a12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01377:Slc16a12
|
APN |
19 |
34,650,084 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL01728:Slc16a12
|
APN |
19 |
34,668,071 (GRCm39) |
missense |
possibly damaging |
0.71 |
PIT1430001:Slc16a12
|
UTSW |
19 |
34,654,759 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0017:Slc16a12
|
UTSW |
19 |
34,650,098 (GRCm39) |
splice site |
probably benign |
|
R0122:Slc16a12
|
UTSW |
19 |
34,652,264 (GRCm39) |
missense |
probably benign |
0.03 |
R0140:Slc16a12
|
UTSW |
19 |
34,650,104 (GRCm39) |
splice site |
probably benign |
|
R1669:Slc16a12
|
UTSW |
19 |
34,657,781 (GRCm39) |
missense |
probably benign |
0.33 |
R4033:Slc16a12
|
UTSW |
19 |
34,652,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R4669:Slc16a12
|
UTSW |
19 |
34,649,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R4703:Slc16a12
|
UTSW |
19 |
34,652,291 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4832:Slc16a12
|
UTSW |
19 |
34,657,780 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4937:Slc16a12
|
UTSW |
19 |
34,652,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R4997:Slc16a12
|
UTSW |
19 |
34,652,358 (GRCm39) |
missense |
probably benign |
0.00 |
R5613:Slc16a12
|
UTSW |
19 |
34,652,358 (GRCm39) |
missense |
probably benign |
0.43 |
R5725:Slc16a12
|
UTSW |
19 |
34,652,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6139:Slc16a12
|
UTSW |
19 |
34,648,295 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6417:Slc16a12
|
UTSW |
19 |
34,650,097 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6420:Slc16a12
|
UTSW |
19 |
34,650,097 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6947:Slc16a12
|
UTSW |
19 |
34,650,007 (GRCm39) |
missense |
probably benign |
0.03 |
R7694:Slc16a12
|
UTSW |
19 |
34,648,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R7819:Slc16a12
|
UTSW |
19 |
34,652,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7860:Slc16a12
|
UTSW |
19 |
34,652,730 (GRCm39) |
missense |
probably benign |
0.00 |
R8882:Slc16a12
|
UTSW |
19 |
34,649,854 (GRCm39) |
missense |
probably benign |
0.01 |
|