Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610010F05Rik |
A |
T |
11: 23,615,265 |
|
probably null |
Het |
3632451O06Rik |
T |
A |
14: 49,770,436 |
T527S |
probably damaging |
Het |
Adck5 |
A |
G |
15: 76,594,335 |
|
probably benign |
Het |
Akr1b3 |
A |
C |
6: 34,304,267 |
|
probably benign |
Het |
Asns |
A |
T |
6: 7,677,978 |
S367T |
probably damaging |
Het |
BC034090 |
T |
C |
1: 155,226,158 |
N120S |
probably benign |
Het |
Bub1 |
A |
T |
2: 127,805,236 |
|
probably benign |
Het |
Csf1 |
T |
A |
3: 107,756,739 |
T38S |
probably damaging |
Het |
Ctsz |
T |
C |
2: 174,428,585 |
E268G |
possibly damaging |
Het |
Dach1 |
G |
A |
14: 97,827,750 |
T685I |
possibly damaging |
Het |
Dclre1a |
A |
G |
19: 56,545,442 |
L240S |
probably benign |
Het |
Ercc1 |
G |
A |
7: 19,347,132 |
|
probably benign |
Het |
Esam |
C |
T |
9: 37,534,196 |
T71I |
probably benign |
Het |
Espl1 |
A |
G |
15: 102,312,989 |
I944V |
probably damaging |
Het |
Gde1 |
A |
G |
7: 118,698,558 |
L35P |
possibly damaging |
Het |
Gm10382 |
A |
G |
5: 125,389,583 |
|
probably benign |
Het |
Hk1 |
C |
A |
10: 62,315,540 |
K10N |
probably damaging |
Het |
Lamc3 |
A |
G |
2: 31,898,232 |
K135E |
probably damaging |
Het |
Lrtm2 |
A |
G |
6: 119,320,528 |
F184S |
probably damaging |
Het |
March11 |
A |
G |
15: 26,309,446 |
E62G |
probably damaging |
Het |
Mtcl1 |
T |
A |
17: 66,380,079 |
T611S |
probably benign |
Het |
Myc |
A |
T |
15: 61,989,664 |
H373L |
probably damaging |
Het |
Myh6 |
T |
A |
14: 54,962,108 |
I249F |
probably damaging |
Het |
Naaa |
T |
C |
5: 92,278,143 |
|
probably benign |
Het |
Nfib |
A |
G |
4: 82,323,658 |
V432A |
probably damaging |
Het |
Nmt1 |
A |
G |
11: 103,043,200 |
K55R |
probably damaging |
Het |
Olfr1228 |
T |
C |
2: 89,249,245 |
R150G |
possibly damaging |
Het |
Opa3 |
C |
T |
7: 19,244,774 |
R55W |
probably damaging |
Het |
Pfn4 |
T |
A |
12: 4,770,182 |
D10E |
probably damaging |
Het |
Pld5 |
T |
A |
1: 176,140,017 |
I91F |
probably damaging |
Het |
Plec |
A |
C |
15: 76,183,117 |
S1350A |
probably damaging |
Het |
Polq |
G |
T |
16: 37,013,181 |
V79F |
probably damaging |
Het |
Ppp1r16b |
T |
C |
2: 158,761,765 |
Y537H |
probably damaging |
Het |
Prdm8 |
T |
C |
5: 98,186,508 |
S645P |
probably damaging |
Het |
Rgs1 |
T |
C |
1: 144,247,906 |
T94A |
probably benign |
Het |
Rpl11 |
G |
A |
4: 136,051,143 |
|
probably benign |
Het |
Scamp3 |
G |
A |
3: 89,181,927 |
|
probably null |
Het |
Sgsm1 |
TTTTATATT |
TTT |
5: 113,258,123 |
|
probably benign |
Het |
Sirpb1b |
A |
T |
3: 15,548,761 |
I87K |
probably damaging |
Het |
Slc14a2 |
G |
A |
18: 78,207,068 |
R62C |
probably damaging |
Het |
Stat4 |
T |
C |
1: 52,071,941 |
|
probably null |
Het |
Tex9 |
A |
T |
9: 72,480,595 |
|
probably null |
Het |
Tsku |
T |
C |
7: 98,352,831 |
T98A |
probably benign |
Het |
Ttc23l |
CT |
CTTGGATT |
15: 10,537,562 |
|
probably benign |
Het |
Ttc23l |
G |
A |
15: 10,537,566 |
S206L |
probably benign |
Het |
Vmn2r116 |
A |
C |
17: 23,401,421 |
I710L |
probably benign |
Het |
Vmn2r16 |
A |
T |
5: 109,363,801 |
I625F |
probably damaging |
Het |
Xpo4 |
G |
A |
14: 57,591,022 |
Q794* |
probably null |
Het |
Zfp112 |
T |
A |
7: 24,125,048 |
I147N |
probably damaging |
Het |
Zmiz1 |
T |
C |
14: 25,636,010 |
S140P |
probably damaging |
Het |
|
Other mutations in H2-M10.6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01018:H2-M10.6
|
APN |
17 |
36,812,220 (GRCm38) |
missense |
probably benign |
0.13 |
IGL01590:H2-M10.6
|
APN |
17 |
36,812,749 (GRCm38) |
missense |
probably benign |
0.05 |
IGL03200:H2-M10.6
|
APN |
17 |
36,814,016 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03278:H2-M10.6
|
APN |
17 |
36,813,823 (GRCm38) |
missense |
probably damaging |
0.99 |
R0018:H2-M10.6
|
UTSW |
17 |
36,814,049 (GRCm38) |
missense |
probably damaging |
1.00 |
R0144:H2-M10.6
|
UTSW |
17 |
36,812,241 (GRCm38) |
missense |
probably damaging |
0.99 |
R0194:H2-M10.6
|
UTSW |
17 |
36,814,042 (GRCm38) |
missense |
probably damaging |
1.00 |
R1168:H2-M10.6
|
UTSW |
17 |
36,813,160 (GRCm38) |
missense |
probably benign |
|
R1757:H2-M10.6
|
UTSW |
17 |
36,813,151 (GRCm38) |
missense |
probably benign |
0.00 |
R1773:H2-M10.6
|
UTSW |
17 |
36,812,184 (GRCm38) |
missense |
probably benign |
0.00 |
R2029:H2-M10.6
|
UTSW |
17 |
36,813,907 (GRCm38) |
missense |
possibly damaging |
0.47 |
R3409:H2-M10.6
|
UTSW |
17 |
36,814,001 (GRCm38) |
missense |
probably damaging |
1.00 |
R3856:H2-M10.6
|
UTSW |
17 |
36,812,504 (GRCm38) |
missense |
probably benign |
0.18 |
R4869:H2-M10.6
|
UTSW |
17 |
36,812,533 (GRCm38) |
missense |
probably benign |
0.04 |
R5684:H2-M10.6
|
UTSW |
17 |
36,813,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R6020:H2-M10.6
|
UTSW |
17 |
36,813,067 (GRCm38) |
missense |
probably damaging |
1.00 |
R6180:H2-M10.6
|
UTSW |
17 |
36,814,286 (GRCm38) |
missense |
probably damaging |
1.00 |
R6328:H2-M10.6
|
UTSW |
17 |
36,813,944 (GRCm38) |
missense |
probably damaging |
0.96 |
R8245:H2-M10.6
|
UTSW |
17 |
36,813,263 (GRCm38) |
critical splice donor site |
probably null |
|
R9687:H2-M10.6
|
UTSW |
17 |
36,814,255 (GRCm38) |
missense |
probably benign |
0.01 |
R9705:H2-M10.6
|
UTSW |
17 |
36,812,750 (GRCm38) |
missense |
probably benign |
0.09 |
|