Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm1 |
T |
C |
4: 144,255,119 (GRCm39) |
Y180H |
possibly damaging |
Het |
Abi3bp |
A |
T |
16: 56,492,336 (GRCm39) |
I1361L |
probably benign |
Het |
Amph |
A |
T |
13: 19,326,172 (GRCm39) |
D634V |
probably damaging |
Het |
Ank1 |
G |
A |
8: 23,583,871 (GRCm39) |
V317I |
possibly damaging |
Het |
Ap4e1 |
G |
A |
2: 126,888,830 (GRCm39) |
V460I |
possibly damaging |
Het |
Arhgap19 |
A |
T |
19: 41,775,016 (GRCm39) |
H198Q |
probably benign |
Het |
Cacna1g |
C |
T |
11: 94,347,937 (GRCm39) |
G717D |
probably damaging |
Het |
Camkk2 |
A |
G |
5: 122,902,013 (GRCm39) |
S99P |
probably damaging |
Het |
Catsperb |
T |
A |
12: 101,475,570 (GRCm39) |
Y371* |
probably null |
Het |
Cbl |
A |
T |
9: 44,065,122 (GRCm39) |
C735* |
probably null |
Het |
Ccdc146 |
C |
A |
5: 21,538,052 (GRCm39) |
A91S |
probably damaging |
Het |
Col1a2 |
G |
T |
6: 4,524,132 (GRCm39) |
D531Y |
probably damaging |
Het |
Dscam |
T |
A |
16: 96,486,550 (GRCm39) |
T1042S |
probably benign |
Het |
Dtnb |
A |
G |
12: 3,782,626 (GRCm39) |
Y363C |
probably benign |
Het |
Ear10 |
A |
G |
14: 44,160,785 (GRCm39) |
L14P |
probably damaging |
Het |
Egf |
A |
G |
3: 129,529,529 (GRCm39) |
S294P |
probably benign |
Het |
Erbb3 |
T |
C |
10: 128,405,237 (GRCm39) |
*1340W |
probably null |
Het |
Fam217b |
A |
G |
2: 178,062,224 (GRCm39) |
T63A |
probably benign |
Het |
Fig4 |
G |
A |
10: 41,108,160 (GRCm39) |
P680L |
possibly damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm6882 |
T |
A |
7: 21,161,512 (GRCm39) |
I119F |
probably damaging |
Het |
Hdac10 |
C |
A |
15: 89,008,736 (GRCm39) |
G442W |
probably damaging |
Het |
Mc2r |
C |
T |
18: 68,540,494 (GRCm39) |
M266I |
possibly damaging |
Het |
Mep1b |
A |
G |
18: 21,228,050 (GRCm39) |
Q551R |
probably benign |
Het |
Mtrf1 |
T |
A |
14: 79,638,948 (GRCm39) |
C27S |
probably benign |
Het |
Myo5c |
T |
A |
9: 75,176,864 (GRCm39) |
M603K |
probably benign |
Het |
Nuf2 |
A |
G |
1: 169,326,407 (GRCm39) |
L448P |
possibly damaging |
Het |
Or10a49 |
C |
T |
7: 108,468,006 (GRCm39) |
M118I |
possibly damaging |
Het |
Or1e30 |
A |
T |
11: 73,678,654 (GRCm39) |
I297L |
probably benign |
Het |
Or2b7 |
T |
C |
13: 21,739,343 (GRCm39) |
N283S |
probably benign |
Het |
Or8g33 |
A |
T |
9: 39,338,025 (GRCm39) |
M114K |
probably damaging |
Het |
Ppp2r5c |
T |
C |
12: 110,534,261 (GRCm39) |
Y375H |
probably benign |
Het |
Pstpip2 |
A |
G |
18: 77,965,325 (GRCm39) |
I317M |
probably benign |
Het |
Pxdn |
A |
G |
12: 30,034,570 (GRCm39) |
T208A |
probably benign |
Het |
Rab3gap1 |
C |
T |
1: 127,818,817 (GRCm39) |
H116Y |
probably damaging |
Het |
Rarb |
T |
A |
14: 16,443,751 (GRCm38) |
D179V |
probably benign |
Het |
Rasal1 |
G |
A |
5: 120,813,488 (GRCm39) |
A621T |
probably damaging |
Het |
Rnf6 |
G |
A |
5: 146,147,717 (GRCm39) |
R434C |
probably damaging |
Het |
Scn10a |
C |
A |
9: 119,464,568 (GRCm39) |
E1011* |
probably null |
Het |
Sec24d |
C |
T |
3: 123,087,244 (GRCm39) |
Q137* |
probably null |
Het |
Slc35g1 |
C |
A |
19: 38,391,642 (GRCm39) |
A308E |
probably damaging |
Het |
Smtnl1 |
C |
A |
2: 84,649,089 (GRCm39) |
C55F |
possibly damaging |
Het |
Sp140l2 |
A |
G |
1: 85,231,907 (GRCm39) |
|
probably benign |
Het |
Stt3a |
A |
T |
9: 36,645,662 (GRCm39) |
D676E |
probably benign |
Het |
Sytl2 |
T |
C |
7: 90,031,047 (GRCm39) |
|
probably benign |
Het |
Trabd2b |
A |
G |
4: 114,266,117 (GRCm39) |
T44A |
probably damaging |
Het |
Tti1 |
A |
T |
2: 157,849,618 (GRCm39) |
D540E |
probably benign |
Het |
Tubgcp6 |
A |
G |
15: 88,987,691 (GRCm39) |
V1094A |
probably benign |
Het |
Vmn1r34 |
A |
G |
6: 66,614,373 (GRCm39) |
Y122H |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Zfp579 |
T |
A |
7: 4,997,257 (GRCm39) |
Q218L |
possibly damaging |
Het |
|
Other mutations in Trim12a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01412:Trim12a
|
APN |
7 |
103,956,202 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02522:Trim12a
|
APN |
7 |
103,950,038 (GRCm39) |
splice site |
probably null |
|
R0900:Trim12a
|
UTSW |
7 |
103,953,469 (GRCm39) |
missense |
probably benign |
0.00 |
R1673:Trim12a
|
UTSW |
7 |
103,955,264 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1856:Trim12a
|
UTSW |
7 |
103,950,064 (GRCm39) |
missense |
probably benign |
0.20 |
R1928:Trim12a
|
UTSW |
7 |
103,956,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R2187:Trim12a
|
UTSW |
7 |
103,953,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R2391:Trim12a
|
UTSW |
7 |
103,956,138 (GRCm39) |
missense |
probably damaging |
0.99 |
R3124:Trim12a
|
UTSW |
7 |
103,950,063 (GRCm39) |
missense |
probably benign |
0.37 |
R3808:Trim12a
|
UTSW |
7 |
103,956,201 (GRCm39) |
missense |
probably benign |
0.05 |
R4409:Trim12a
|
UTSW |
7 |
103,956,201 (GRCm39) |
missense |
probably benign |
0.05 |
R4951:Trim12a
|
UTSW |
7 |
103,953,565 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5325:Trim12a
|
UTSW |
7 |
103,953,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5694:Trim12a
|
UTSW |
7 |
103,956,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R6376:Trim12a
|
UTSW |
7 |
103,955,241 (GRCm39) |
missense |
probably benign |
0.03 |
R7002:Trim12a
|
UTSW |
7 |
103,953,383 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7443:Trim12a
|
UTSW |
7 |
103,950,049 (GRCm39) |
missense |
probably damaging |
0.99 |
R7980:Trim12a
|
UTSW |
7 |
103,953,335 (GRCm39) |
missense |
probably benign |
0.36 |
R8284:Trim12a
|
UTSW |
7 |
103,955,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R8412:Trim12a
|
UTSW |
7 |
103,953,544 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8509:Trim12a
|
UTSW |
7 |
103,955,234 (GRCm39) |
missense |
probably benign |
0.00 |
R8995:Trim12a
|
UTSW |
7 |
103,953,532 (GRCm39) |
missense |
probably benign |
0.04 |
R9509:Trim12a
|
UTSW |
7 |
103,953,551 (GRCm39) |
missense |
probably benign |
0.06 |
|