Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
A |
G |
12: 118,865,184 (GRCm39) |
|
probably benign |
Het |
Abcf2 |
A |
T |
5: 24,772,268 (GRCm39) |
Y487N |
probably damaging |
Het |
Adcy4 |
T |
C |
14: 56,021,056 (GRCm39) |
Y27C |
probably damaging |
Het |
Atp2a2 |
T |
C |
5: 122,609,299 (GRCm39) |
I188V |
probably benign |
Het |
Cacna1s |
A |
T |
1: 136,040,695 (GRCm39) |
I1231F |
possibly damaging |
Het |
Capn7 |
T |
A |
14: 31,091,714 (GRCm39) |
C704S |
possibly damaging |
Het |
Celsr2 |
G |
T |
3: 108,308,617 (GRCm39) |
T1770K |
possibly damaging |
Het |
Chmp7 |
C |
T |
14: 69,956,899 (GRCm39) |
M336I |
probably benign |
Het |
Cul9 |
T |
C |
17: 46,848,748 (GRCm39) |
|
probably null |
Het |
Dpp10 |
A |
G |
1: 123,360,658 (GRCm39) |
|
probably null |
Het |
Dscaml1 |
A |
G |
9: 45,656,372 (GRCm39) |
I1571V |
probably benign |
Het |
Eif3j2 |
T |
A |
18: 43,610,036 (GRCm39) |
Y259F |
probably benign |
Het |
Erc2 |
A |
C |
14: 27,747,105 (GRCm39) |
N345T |
probably benign |
Het |
Fbxo21 |
T |
C |
5: 118,133,573 (GRCm39) |
|
probably benign |
Het |
Frmd8 |
A |
T |
19: 5,915,084 (GRCm39) |
|
probably benign |
Het |
Gfm1 |
T |
C |
3: 67,381,928 (GRCm39) |
S705P |
probably damaging |
Het |
Gucy1b2 |
T |
C |
14: 62,656,511 (GRCm39) |
D282G |
probably benign |
Het |
H2-Ab1 |
T |
C |
17: 34,486,328 (GRCm39) |
I129T |
probably damaging |
Het |
Lipm |
A |
T |
19: 34,096,161 (GRCm39) |
T326S |
probably benign |
Het |
Lrrc8c |
T |
C |
5: 105,756,400 (GRCm39) |
L725P |
probably damaging |
Het |
Map3k19 |
A |
G |
1: 127,762,375 (GRCm39) |
|
probably benign |
Het |
Med31 |
T |
A |
11: 72,104,657 (GRCm39) |
N50I |
probably damaging |
Het |
Myo15b |
T |
G |
11: 115,757,162 (GRCm39) |
|
probably benign |
Het |
Nemp1 |
T |
C |
10: 127,528,893 (GRCm39) |
L199S |
probably damaging |
Het |
Nod2 |
G |
A |
8: 89,399,290 (GRCm39) |
|
probably benign |
Het |
Oga |
C |
T |
19: 45,771,425 (GRCm39) |
A49T |
probably benign |
Het |
Or2ak6 |
A |
G |
11: 58,593,435 (GRCm39) |
R303G |
possibly damaging |
Het |
Or5b21 |
A |
G |
19: 12,840,008 (GRCm39) |
I290V |
probably benign |
Het |
Parva |
G |
A |
7: 112,167,071 (GRCm39) |
V215M |
probably damaging |
Het |
Phf1 |
T |
C |
17: 27,156,114 (GRCm39) |
|
probably benign |
Het |
Plscr1l1 |
A |
T |
9: 92,233,140 (GRCm39) |
I88L |
possibly damaging |
Het |
Ppp1r12c |
G |
T |
7: 4,489,365 (GRCm39) |
Q240K |
probably damaging |
Het |
Ralgapa1 |
A |
T |
12: 55,809,466 (GRCm39) |
Y436* |
probably null |
Het |
Ralgapa1 |
C |
A |
12: 55,829,562 (GRCm39) |
|
probably benign |
Het |
Rbm11 |
C |
T |
16: 75,393,525 (GRCm39) |
R74C |
probably damaging |
Het |
Robo3 |
A |
G |
9: 37,333,479 (GRCm39) |
V744A |
probably damaging |
Het |
Rsbn1 |
T |
G |
3: 103,861,469 (GRCm39) |
S522A |
probably damaging |
Het |
Scel |
T |
A |
14: 103,823,916 (GRCm39) |
S381R |
possibly damaging |
Het |
Sec31b |
G |
A |
19: 44,506,612 (GRCm39) |
Q909* |
probably null |
Het |
Slc38a11 |
T |
A |
2: 65,184,124 (GRCm39) |
I176L |
possibly damaging |
Het |
Slc39a4 |
C |
T |
15: 76,496,839 (GRCm39) |
D574N |
probably damaging |
Het |
Slc44a1 |
T |
G |
4: 53,536,421 (GRCm39) |
V199G |
possibly damaging |
Het |
Sltm |
A |
G |
9: 70,469,190 (GRCm39) |
T150A |
probably benign |
Het |
Son |
C |
A |
16: 91,452,372 (GRCm39) |
A373D |
probably damaging |
Het |
Sp140 |
C |
T |
1: 85,547,772 (GRCm39) |
|
probably benign |
Het |
Speg |
A |
G |
1: 75,392,036 (GRCm39) |
Y1606C |
probably damaging |
Het |
Srgap1 |
A |
T |
10: 121,621,379 (GRCm39) |
V1061D |
probably damaging |
Het |
Stat5a |
A |
G |
11: 100,765,908 (GRCm39) |
|
probably null |
Het |
Supt4a |
T |
A |
11: 87,628,409 (GRCm39) |
|
probably benign |
Het |
Teddm1b |
A |
G |
1: 153,750,638 (GRCm39) |
K149R |
possibly damaging |
Het |
Thnsl2 |
A |
T |
6: 71,111,208 (GRCm39) |
L220* |
probably null |
Het |
Tinf2 |
G |
A |
14: 55,917,566 (GRCm39) |
P308S |
probably benign |
Het |
Tmem131l |
A |
G |
3: 83,847,879 (GRCm39) |
S329P |
probably benign |
Het |
Tnf |
T |
C |
17: 35,420,120 (GRCm39) |
|
probably benign |
Het |
Upp2 |
A |
G |
2: 58,661,568 (GRCm39) |
T144A |
probably benign |
Het |
Vmn2r94 |
T |
G |
17: 18,477,973 (GRCm39) |
Q146P |
probably damaging |
Het |
Zfhx4 |
T |
A |
3: 5,310,375 (GRCm39) |
S919R |
possibly damaging |
Het |
|
Other mutations in H2-M10.3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02223:H2-M10.3
|
APN |
17 |
36,678,972 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02410:H2-M10.3
|
APN |
17 |
36,677,428 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02625:H2-M10.3
|
APN |
17 |
36,678,417 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03218:H2-M10.3
|
APN |
17 |
36,678,279 (GRCm39) |
missense |
probably damaging |
0.99 |
R0863:H2-M10.3
|
UTSW |
17 |
36,677,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:H2-M10.3
|
UTSW |
17 |
36,677,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1737:H2-M10.3
|
UTSW |
17 |
36,679,296 (GRCm39) |
missense |
probably benign |
0.22 |
R1833:H2-M10.3
|
UTSW |
17 |
36,678,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:H2-M10.3
|
UTSW |
17 |
36,678,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4515:H2-M10.3
|
UTSW |
17 |
36,678,722 (GRCm39) |
splice site |
probably null |
|
R4517:H2-M10.3
|
UTSW |
17 |
36,678,722 (GRCm39) |
splice site |
probably null |
|
R4519:H2-M10.3
|
UTSW |
17 |
36,678,722 (GRCm39) |
splice site |
probably null |
|
R4834:H2-M10.3
|
UTSW |
17 |
36,678,286 (GRCm39) |
missense |
probably benign |
0.28 |
R4863:H2-M10.3
|
UTSW |
17 |
36,677,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R5473:H2-M10.3
|
UTSW |
17 |
36,678,261 (GRCm39) |
missense |
probably damaging |
0.97 |
R6038:H2-M10.3
|
UTSW |
17 |
36,679,287 (GRCm39) |
missense |
probably benign |
0.15 |
R6038:H2-M10.3
|
UTSW |
17 |
36,679,287 (GRCm39) |
missense |
probably benign |
0.15 |
R7192:H2-M10.3
|
UTSW |
17 |
36,677,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R7515:H2-M10.3
|
UTSW |
17 |
36,677,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:H2-M10.3
|
UTSW |
17 |
36,677,174 (GRCm39) |
missense |
probably benign |
0.38 |
R9198:H2-M10.3
|
UTSW |
17 |
36,678,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R9487:H2-M10.3
|
UTSW |
17 |
36,677,423 (GRCm39) |
missense |
probably benign |
0.42 |
Z1177:H2-M10.3
|
UTSW |
17 |
36,678,436 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:H2-M10.3
|
UTSW |
17 |
36,677,471 (GRCm39) |
missense |
probably damaging |
1.00 |
|