Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,399,470 |
|
probably benign |
Het |
Abcb5 |
T |
A |
12: 118,918,200 |
D598V |
probably damaging |
Het |
Adssl1 |
T |
C |
12: 112,634,736 |
|
probably benign |
Het |
Akap9 |
T |
A |
5: 3,970,711 |
S1141T |
probably benign |
Het |
Avil |
T |
C |
10: 127,017,034 |
|
probably null |
Het |
Avl9 |
C |
A |
6: 56,725,090 |
H77N |
probably damaging |
Het |
Cacna1e |
A |
G |
1: 154,443,907 |
V1349A |
probably damaging |
Het |
Cdc23 |
A |
C |
18: 34,634,644 |
S483A |
probably benign |
Het |
Cep192 |
C |
T |
18: 67,858,903 |
P1951S |
probably benign |
Het |
Cp |
A |
G |
3: 19,966,367 |
T175A |
probably damaging |
Het |
Dubr |
A |
C |
16: 50,732,635 |
|
noncoding transcript |
Het |
Eif4g2 |
G |
T |
7: 111,074,713 |
Q695K |
possibly damaging |
Het |
Endod1 |
A |
T |
9: 14,357,239 |
S317T |
possibly damaging |
Het |
Ep400 |
T |
C |
5: 110,742,048 |
T450A |
probably benign |
Het |
Erc1 |
A |
C |
6: 119,722,303 |
V790G |
probably damaging |
Het |
Fam222a |
T |
A |
5: 114,594,453 |
L23Q |
possibly damaging |
Het |
Fam35a |
C |
T |
14: 34,259,727 |
V485I |
probably benign |
Het |
Fancf |
A |
G |
7: 51,861,287 |
V323A |
probably benign |
Het |
Grik2 |
T |
A |
10: 49,244,330 |
Q621L |
probably damaging |
Het |
Gsk3b |
G |
T |
16: 38,220,018 |
R319L |
probably benign |
Het |
Ikzf1 |
A |
G |
11: 11,768,923 |
Y297C |
probably damaging |
Het |
Katnal2 |
T |
C |
18: 77,047,167 |
|
probably benign |
Het |
Lrba |
G |
T |
3: 86,295,400 |
C289F |
probably damaging |
Het |
Mos |
T |
C |
4: 3,871,815 |
|
probably benign |
Het |
Mycn |
T |
C |
12: 12,937,586 |
D270G |
possibly damaging |
Het |
Olfr672 |
A |
T |
7: 104,996,721 |
M61K |
probably damaging |
Het |
Olfr777 |
T |
A |
10: 129,268,523 |
I267F |
probably benign |
Het |
Pclo |
A |
G |
5: 14,675,999 |
|
probably benign |
Het |
Pgm2 |
A |
G |
4: 99,929,606 |
D14G |
probably damaging |
Het |
Pramel7 |
T |
A |
2: 87,491,373 |
D106V |
possibly damaging |
Het |
Prdm9 |
G |
T |
17: 15,553,346 |
H263N |
probably benign |
Het |
Psd4 |
T |
A |
2: 24,396,787 |
|
probably null |
Het |
Ptprc |
G |
A |
1: 138,099,631 |
T493I |
possibly damaging |
Het |
Rbbp8 |
T |
A |
18: 11,721,979 |
S420R |
probably benign |
Het |
Sap30bp |
A |
G |
11: 115,962,547 |
T219A |
probably damaging |
Het |
Slc2a7 |
T |
A |
4: 150,157,564 |
L200Q |
probably damaging |
Het |
Slc38a6 |
T |
A |
12: 73,288,525 |
|
probably null |
Het |
Tatdn2 |
T |
A |
6: 113,704,024 |
|
probably benign |
Het |
Thrb |
A |
G |
14: 18,011,056 |
|
probably benign |
Het |
Timp4 |
T |
C |
6: 115,246,308 |
Y218C |
possibly damaging |
Het |
Tlr5 |
A |
G |
1: 182,974,748 |
D525G |
probably benign |
Het |
Usp32 |
G |
T |
11: 84,988,482 |
T1467N |
probably benign |
Het |
Zbtb43 |
T |
C |
2: 33,454,091 |
H374R |
probably benign |
Het |
Zfhx4 |
C |
A |
3: 5,243,568 |
T618K |
probably damaging |
Het |
|