Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
G |
A |
5: 64,053,826 (GRCm39) |
S11N |
probably null |
Het |
Aqp9 |
T |
C |
9: 71,030,188 (GRCm39) |
I200V |
possibly damaging |
Het |
Cntn2 |
T |
C |
1: 132,453,059 (GRCm39) |
E411G |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Cstdc5 |
C |
A |
16: 36,187,848 (GRCm39) |
V6F |
possibly damaging |
Het |
Dennd3 |
A |
G |
15: 73,438,905 (GRCm39) |
D1091G |
probably damaging |
Het |
Dock2 |
T |
C |
11: 34,589,567 (GRCm39) |
|
probably benign |
Het |
Dscam |
T |
A |
16: 96,442,097 (GRCm39) |
I1577F |
probably benign |
Het |
Egflam |
A |
T |
15: 7,279,559 (GRCm39) |
N482K |
probably benign |
Het |
Fam216a |
T |
C |
5: 122,505,574 (GRCm39) |
T129A |
probably damaging |
Het |
Fbxo40 |
T |
C |
16: 36,790,136 (GRCm39) |
M325V |
probably benign |
Het |
Fbxw8 |
C |
T |
5: 118,267,020 (GRCm39) |
V148M |
possibly damaging |
Het |
Fcgbp |
C |
T |
7: 27,774,596 (GRCm39) |
R57C |
probably damaging |
Het |
Gnpnat1 |
A |
G |
14: 45,618,388 (GRCm39) |
|
probably null |
Het |
Gria2 |
T |
C |
3: 80,616,729 (GRCm39) |
T408A |
probably benign |
Het |
H2-T3 |
A |
G |
17: 36,497,500 (GRCm39) |
M59T |
probably benign |
Het |
Jakmip1 |
C |
T |
5: 37,258,187 (GRCm39) |
Q278* |
probably null |
Het |
Krtap21-1 |
C |
T |
16: 89,200,312 (GRCm39) |
G110D |
unknown |
Het |
Myo7a |
C |
T |
7: 97,756,198 (GRCm39) |
|
probably null |
Het |
Nlrp9c |
T |
A |
7: 26,093,632 (GRCm39) |
Q11L |
probably benign |
Het |
Or14a257 |
A |
G |
7: 86,138,336 (GRCm39) |
L141P |
probably damaging |
Het |
Or5b94 |
A |
T |
19: 12,651,899 (GRCm39) |
D110V |
probably benign |
Het |
Or6c75 |
T |
A |
10: 129,336,939 (GRCm39) |
M62K |
probably benign |
Het |
Or6c8 |
A |
C |
10: 128,915,099 (GRCm39) |
I244M |
probably damaging |
Het |
Pdzd8 |
A |
G |
19: 59,289,825 (GRCm39) |
I525T |
probably benign |
Het |
Pign |
A |
T |
1: 105,574,506 (GRCm39) |
L280* |
probably null |
Het |
Pik3r4 |
T |
G |
9: 105,527,530 (GRCm39) |
I294M |
possibly damaging |
Het |
Pkhd1 |
T |
A |
1: 20,187,944 (GRCm39) |
I3455F |
probably damaging |
Het |
Prmt3 |
C |
T |
7: 49,498,506 (GRCm39) |
Q471* |
probably null |
Het |
Prrc2c |
A |
G |
1: 162,520,439 (GRCm39) |
F2006L |
probably damaging |
Het |
Ptger3 |
C |
T |
3: 157,272,808 (GRCm39) |
R52C |
probably damaging |
Het |
Rfx2 |
T |
C |
17: 57,115,325 (GRCm39) |
|
probably benign |
Het |
Sh3bp4 |
T |
C |
1: 89,072,870 (GRCm39) |
F573L |
probably damaging |
Het |
Slc18a2 |
G |
T |
19: 59,251,733 (GRCm39) |
|
probably benign |
Het |
Slc26a8 |
T |
A |
17: 28,857,624 (GRCm39) |
I840F |
probably benign |
Het |
Slc5a4b |
A |
T |
10: 75,908,299 (GRCm39) |
Y364* |
probably null |
Het |
Slitrk1 |
A |
G |
14: 109,149,754 (GRCm39) |
I319T |
probably benign |
Het |
Stxbp5l |
C |
T |
16: 37,028,567 (GRCm39) |
A499T |
probably benign |
Het |
Tnks2 |
T |
A |
19: 36,861,503 (GRCm39) |
S951R |
probably benign |
Het |
Tyro3 |
C |
T |
2: 119,635,345 (GRCm39) |
|
probably benign |
Het |
Vmn1r34 |
A |
T |
6: 66,614,042 (GRCm39) |
L232Q |
probably damaging |
Het |
Zfp148 |
T |
A |
16: 33,315,816 (GRCm39) |
C215S |
probably damaging |
Het |
Zzef1 |
C |
T |
11: 72,782,043 (GRCm39) |
P1995S |
probably benign |
Het |
Zzef1 |
T |
A |
11: 72,790,364 (GRCm39) |
V2106D |
possibly damaging |
Het |
|
Other mutations in Trim30c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00467:Trim30c
|
APN |
7 |
104,031,389 (GRCm39) |
nonsense |
probably null |
|
IGL00573:Trim30c
|
APN |
7 |
104,031,838 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01023:Trim30c
|
APN |
7 |
104,032,179 (GRCm39) |
splice site |
probably benign |
|
IGL01413:Trim30c
|
APN |
7 |
104,031,541 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01418:Trim30c
|
APN |
7 |
104,031,541 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02330:Trim30c
|
APN |
7 |
104,032,165 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03107:Trim30c
|
APN |
7 |
104,031,820 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0195:Trim30c
|
UTSW |
7 |
104,031,636 (GRCm39) |
missense |
probably benign |
|
R0324:Trim30c
|
UTSW |
7 |
104,032,516 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0826:Trim30c
|
UTSW |
7 |
104,032,688 (GRCm39) |
missense |
probably benign |
0.01 |
R0865:Trim30c
|
UTSW |
7 |
104,039,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Trim30c
|
UTSW |
7 |
104,032,459 (GRCm39) |
missense |
probably benign |
0.00 |
R1513:Trim30c
|
UTSW |
7 |
104,031,896 (GRCm39) |
missense |
probably benign |
0.04 |
R1563:Trim30c
|
UTSW |
7 |
104,032,158 (GRCm39) |
missense |
probably benign |
0.00 |
R2220:Trim30c
|
UTSW |
7 |
104,032,474 (GRCm39) |
missense |
probably benign |
|
R2442:Trim30c
|
UTSW |
7 |
104,031,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R5326:Trim30c
|
UTSW |
7 |
104,037,511 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5777:Trim30c
|
UTSW |
7 |
104,032,538 (GRCm39) |
missense |
probably benign |
0.08 |
R6118:Trim30c
|
UTSW |
7 |
104,031,288 (GRCm39) |
missense |
probably benign |
0.01 |
R6257:Trim30c
|
UTSW |
7 |
104,039,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6374:Trim30c
|
UTSW |
7 |
104,039,609 (GRCm39) |
missense |
probably benign |
0.01 |
R7387:Trim30c
|
UTSW |
7 |
104,039,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R7419:Trim30c
|
UTSW |
7 |
104,037,472 (GRCm39) |
missense |
probably benign |
0.11 |
R7500:Trim30c
|
UTSW |
7 |
104,036,758 (GRCm39) |
missense |
probably benign |
0.00 |
R7542:Trim30c
|
UTSW |
7 |
104,031,425 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8207:Trim30c
|
UTSW |
7 |
104,032,703 (GRCm39) |
missense |
probably benign |
|
R8501:Trim30c
|
UTSW |
7 |
104,036,677 (GRCm39) |
missense |
probably benign |
|
R9059:Trim30c
|
UTSW |
7 |
104,031,272 (GRCm39) |
makesense |
probably null |
|
R9193:Trim30c
|
UTSW |
7 |
104,031,553 (GRCm39) |
missense |
probably benign |
0.23 |
Z1176:Trim30c
|
UTSW |
7 |
104,032,465 (GRCm39) |
missense |
probably damaging |
0.96 |
|