Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578I06Rik |
A |
T |
14: 64,208,569 (GRCm39) |
|
probably null |
Het |
Agbl4 |
T |
G |
4: 111,383,798 (GRCm39) |
S218A |
probably benign |
Het |
Apol11b |
T |
C |
15: 77,522,153 (GRCm39) |
E48G |
probably damaging |
Het |
Atp4a |
T |
A |
7: 30,419,666 (GRCm39) |
N676K |
probably benign |
Het |
Capn5 |
T |
A |
7: 97,775,574 (GRCm39) |
S456C |
probably benign |
Het |
Ccar1 |
T |
C |
10: 62,600,161 (GRCm39) |
Y590C |
probably damaging |
Het |
Ccdc188 |
G |
T |
16: 18,037,070 (GRCm39) |
G283W |
probably damaging |
Het |
Cd69 |
A |
G |
6: 129,248,351 (GRCm39) |
V45A |
probably damaging |
Het |
Col3a1 |
G |
T |
1: 45,377,771 (GRCm39) |
|
probably benign |
Het |
Cyb561a3 |
A |
T |
19: 10,564,166 (GRCm39) |
T169S |
probably benign |
Het |
Cyp2c39 |
A |
T |
19: 39,527,397 (GRCm39) |
I248L |
probably benign |
Het |
Cyp2j13 |
T |
C |
4: 95,947,344 (GRCm39) |
T236A |
possibly damaging |
Het |
Efs |
A |
G |
14: 55,154,961 (GRCm39) |
V426A |
probably benign |
Het |
Eme2 |
A |
G |
17: 25,113,157 (GRCm39) |
L136S |
probably damaging |
Het |
Fastkd1 |
T |
A |
2: 69,535,872 (GRCm39) |
K312* |
probably null |
Het |
Fbxl12 |
A |
G |
9: 20,553,530 (GRCm39) |
L19P |
probably damaging |
Het |
Flg2 |
T |
A |
3: 93,110,913 (GRCm39) |
Y980* |
probably null |
Het |
Fscn2 |
T |
A |
11: 120,257,527 (GRCm39) |
I296N |
probably damaging |
Het |
Gabrg3 |
A |
G |
7: 56,384,835 (GRCm39) |
V242A |
probably benign |
Het |
Galk2 |
A |
G |
2: 125,817,315 (GRCm39) |
H368R |
probably damaging |
Het |
Gm12695 |
C |
T |
4: 96,657,893 (GRCm39) |
S92N |
probably benign |
Het |
Gpalpp1 |
A |
T |
14: 76,336,031 (GRCm39) |
S196T |
probably benign |
Het |
Gpld1 |
A |
T |
13: 25,168,804 (GRCm39) |
M773L |
probably benign |
Het |
Haus8 |
A |
G |
8: 71,708,289 (GRCm39) |
|
probably null |
Het |
Hirip3 |
A |
G |
7: 126,462,038 (GRCm39) |
R19G |
probably damaging |
Het |
Inpp4a |
A |
G |
1: 37,405,247 (GRCm39) |
T92A |
probably damaging |
Het |
Irgm2 |
A |
G |
11: 58,111,218 (GRCm39) |
D303G |
probably damaging |
Het |
Kpna2rt |
C |
A |
17: 90,217,697 (GRCm39) |
R16S |
probably benign |
Het |
Krtap5-2 |
T |
G |
7: 141,728,748 (GRCm39) |
S311R |
unknown |
Het |
Krtdap |
T |
A |
7: 30,489,185 (GRCm39) |
|
probably null |
Het |
Lce1g |
G |
T |
3: 92,658,140 (GRCm39) |
S56Y |
unknown |
Het |
Lrrn1 |
G |
A |
6: 107,545,794 (GRCm39) |
V531I |
probably benign |
Het |
Mctp2 |
T |
C |
7: 71,861,358 (GRCm39) |
E429G |
probably damaging |
Het |
Mrgpra2b |
T |
G |
7: 47,113,793 (GRCm39) |
D287A |
probably damaging |
Het |
Mterf3 |
T |
C |
13: 67,076,258 (GRCm39) |
T150A |
probably damaging |
Het |
Mtus2 |
A |
G |
5: 148,014,725 (GRCm39) |
N506S |
probably benign |
Het |
Myh15 |
G |
T |
16: 48,963,313 (GRCm39) |
V1085L |
probably benign |
Het |
Myo9a |
A |
G |
9: 59,687,048 (GRCm39) |
N51S |
probably benign |
Het |
Nlrc3 |
A |
T |
16: 3,771,304 (GRCm39) |
L196Q |
probably damaging |
Het |
Nlrp9c |
T |
A |
7: 26,074,747 (GRCm39) |
N816I |
probably damaging |
Het |
Nt5dc1 |
T |
C |
10: 34,189,673 (GRCm39) |
E339G |
possibly damaging |
Het |
Or10ak14 |
C |
T |
4: 118,611,331 (GRCm39) |
V135I |
probably benign |
Het |
Or51b6b |
A |
G |
7: 103,309,779 (GRCm39) |
V226A |
probably damaging |
Het |
Or8j3c |
A |
T |
2: 86,253,165 (GRCm39) |
L285* |
probably null |
Het |
Pik3ap1 |
A |
G |
19: 41,284,828 (GRCm39) |
I619T |
probably damaging |
Het |
Plk1 |
A |
G |
7: 121,759,118 (GRCm39) |
D118G |
probably benign |
Het |
Ppat |
T |
C |
5: 77,070,314 (GRCm39) |
D168G |
possibly damaging |
Het |
Preb |
T |
C |
5: 31,115,849 (GRCm39) |
E198G |
probably damaging |
Het |
Psg21 |
T |
C |
7: 18,386,378 (GRCm39) |
T203A |
possibly damaging |
Het |
Rbm17 |
A |
G |
2: 11,602,942 (GRCm39) |
V54A |
probably damaging |
Het |
Rgma |
T |
A |
7: 73,067,574 (GRCm39) |
D276E |
probably damaging |
Het |
Ric8a |
T |
C |
7: 140,439,471 (GRCm39) |
L77P |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Scarf1 |
A |
C |
11: 75,416,854 (GRCm39) |
E765D |
probably damaging |
Het |
Scart1 |
A |
T |
7: 139,803,890 (GRCm39) |
N363Y |
possibly damaging |
Het |
Sec14l4 |
G |
A |
11: 3,990,041 (GRCm39) |
M113I |
probably benign |
Het |
Senp1 |
C |
T |
15: 97,980,165 (GRCm39) |
C60Y |
probably damaging |
Het |
Slc22a21 |
T |
A |
11: 53,842,130 (GRCm39) |
K549N |
probably benign |
Het |
Slc39a10 |
T |
C |
1: 46,875,156 (GRCm39) |
S49G |
probably damaging |
Het |
Spata13 |
T |
C |
14: 60,947,004 (GRCm39) |
M684T |
probably damaging |
Het |
Spns1 |
T |
C |
7: 125,969,958 (GRCm39) |
T481A |
probably damaging |
Het |
Stag1 |
A |
G |
9: 100,668,666 (GRCm39) |
Y198C |
possibly damaging |
Het |
Tgfbr1 |
T |
A |
4: 47,402,833 (GRCm39) |
V210E |
probably damaging |
Het |
Tnc |
C |
T |
4: 63,893,475 (GRCm39) |
E1604K |
possibly damaging |
Het |
Tspan31 |
T |
C |
10: 126,904,365 (GRCm39) |
D143G |
probably benign |
Het |
Tspan5 |
T |
A |
3: 138,603,903 (GRCm39) |
Y131* |
probably null |
Het |
Ttc21a |
A |
G |
9: 119,795,189 (GRCm39) |
D1070G |
probably damaging |
Het |
Vmn2r26 |
C |
T |
6: 124,016,708 (GRCm39) |
P391S |
probably benign |
Het |
Vmn2r72 |
A |
G |
7: 85,387,464 (GRCm39) |
I700T |
probably damaging |
Het |
Vps13c |
A |
C |
9: 67,821,102 (GRCm39) |
N1204T |
probably damaging |
Het |
Zfhx4 |
C |
T |
3: 5,468,418 (GRCm39) |
P2859S |
probably benign |
Het |
|
Other mutations in Nsun2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01660:Nsun2
|
APN |
13 |
69,771,368 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01997:Nsun2
|
APN |
13 |
69,771,365 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02253:Nsun2
|
APN |
13 |
69,767,658 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03038:Nsun2
|
APN |
13 |
69,767,703 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02984:Nsun2
|
UTSW |
13 |
69,691,727 (GRCm39) |
intron |
probably benign |
|
PIT4494001:Nsun2
|
UTSW |
13 |
69,766,311 (GRCm39) |
critical splice donor site |
probably null |
|
R0601:Nsun2
|
UTSW |
13 |
69,781,361 (GRCm39) |
missense |
probably benign |
0.40 |
R0648:Nsun2
|
UTSW |
13 |
69,775,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Nsun2
|
UTSW |
13 |
69,777,661 (GRCm39) |
missense |
probably benign |
|
R0718:Nsun2
|
UTSW |
13 |
69,691,816 (GRCm39) |
intron |
probably benign |
|
R1501:Nsun2
|
UTSW |
13 |
69,779,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1638:Nsun2
|
UTSW |
13 |
69,775,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R1678:Nsun2
|
UTSW |
13 |
69,775,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R1687:Nsun2
|
UTSW |
13 |
69,775,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Nsun2
|
UTSW |
13 |
69,777,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Nsun2
|
UTSW |
13 |
69,777,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R3689:Nsun2
|
UTSW |
13 |
69,760,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R3691:Nsun2
|
UTSW |
13 |
69,760,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R3739:Nsun2
|
UTSW |
13 |
69,777,757 (GRCm39) |
missense |
probably benign |
|
R3918:Nsun2
|
UTSW |
13 |
69,778,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4065:Nsun2
|
UTSW |
13 |
69,760,579 (GRCm39) |
critical splice donor site |
probably null |
|
R4231:Nsun2
|
UTSW |
13 |
69,767,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R4445:Nsun2
|
UTSW |
13 |
69,777,840 (GRCm39) |
splice site |
probably null |
|
R4872:Nsun2
|
UTSW |
13 |
69,691,992 (GRCm39) |
intron |
probably benign |
|
R5641:Nsun2
|
UTSW |
13 |
69,771,368 (GRCm39) |
missense |
probably benign |
0.01 |
R5718:Nsun2
|
UTSW |
13 |
69,771,403 (GRCm39) |
missense |
probably benign |
0.19 |
R5976:Nsun2
|
UTSW |
13 |
69,771,271 (GRCm39) |
splice site |
probably null |
|
R6110:Nsun2
|
UTSW |
13 |
69,775,767 (GRCm39) |
missense |
probably benign |
0.01 |
R6943:Nsun2
|
UTSW |
13 |
69,778,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Nsun2
|
UTSW |
13 |
69,779,409 (GRCm39) |
missense |
probably benign |
0.00 |
R7146:Nsun2
|
UTSW |
13 |
69,774,672 (GRCm39) |
critical splice donor site |
probably null |
|
R7456:Nsun2
|
UTSW |
13 |
69,781,725 (GRCm39) |
missense |
probably damaging |
0.98 |
R8017:Nsun2
|
UTSW |
13 |
69,775,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R8019:Nsun2
|
UTSW |
13 |
69,775,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R8225:Nsun2
|
UTSW |
13 |
69,760,493 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8935:Nsun2
|
UTSW |
13 |
69,767,586 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Nsun2
|
UTSW |
13 |
69,763,638 (GRCm39) |
critical splice donor site |
probably null |
|
Z1088:Nsun2
|
UTSW |
13 |
69,763,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|