Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
A |
9: 124,056,679 (GRCm39) |
T103S |
probably benign |
Het |
Aadacl2fm3 |
A |
G |
3: 59,784,400 (GRCm39) |
Y291C |
probably damaging |
Het |
Aass |
A |
T |
6: 23,075,261 (GRCm39) |
|
probably benign |
Het |
Adgrb3 |
A |
T |
1: 25,133,235 (GRCm39) |
C1284S |
probably damaging |
Het |
Adora2a |
G |
A |
10: 75,169,559 (GRCm39) |
W341* |
probably null |
Het |
Afg2a |
T |
A |
3: 37,486,142 (GRCm39) |
L288H |
probably damaging |
Het |
Arap1 |
G |
A |
7: 101,057,324 (GRCm39) |
R1355Q |
possibly damaging |
Het |
Asic5 |
A |
T |
3: 81,913,915 (GRCm39) |
|
probably benign |
Het |
Canx |
T |
C |
11: 50,195,270 (GRCm39) |
D266G |
possibly damaging |
Het |
Cfap57 |
A |
T |
4: 118,426,799 (GRCm39) |
Y1080N |
probably damaging |
Het |
Chat |
C |
T |
14: 32,130,963 (GRCm39) |
M559I |
probably benign |
Het |
Chd5 |
G |
A |
4: 152,463,305 (GRCm39) |
S1425N |
possibly damaging |
Het |
Cog8 |
T |
C |
8: 107,783,202 (GRCm39) |
D29G |
probably damaging |
Het |
Cox15 |
A |
G |
19: 43,732,172 (GRCm39) |
S215P |
probably benign |
Het |
Cramp1 |
C |
T |
17: 25,202,114 (GRCm39) |
G456D |
probably damaging |
Het |
Dbt |
T |
C |
3: 116,339,698 (GRCm39) |
V362A |
probably damaging |
Het |
Dio1 |
C |
A |
4: 107,164,147 (GRCm39) |
A57S |
probably benign |
Het |
F5 |
C |
A |
1: 164,026,440 (GRCm39) |
H1671N |
probably benign |
Het |
Gm6309 |
A |
G |
5: 146,107,155 (GRCm39) |
Y64H |
probably damaging |
Het |
Hipk1 |
A |
G |
3: 103,660,743 (GRCm39) |
C731R |
probably damaging |
Het |
Hmgcl |
G |
A |
4: 135,683,015 (GRCm39) |
A156T |
probably damaging |
Het |
Il15ra |
A |
T |
2: 11,737,995 (GRCm39) |
T210S |
possibly damaging |
Het |
Kat8 |
T |
C |
7: 127,524,400 (GRCm39) |
L426P |
probably damaging |
Het |
Lrrc39 |
G |
T |
3: 116,359,496 (GRCm39) |
V14L |
probably damaging |
Het |
Lrrc7 |
T |
C |
3: 157,869,593 (GRCm39) |
M709V |
probably benign |
Het |
Mdm4 |
T |
C |
1: 132,919,671 (GRCm39) |
H398R |
probably benign |
Het |
Mroh2b |
A |
T |
15: 4,991,606 (GRCm39) |
Q1568L |
possibly damaging |
Het |
Myo18b |
G |
A |
5: 113,022,795 (GRCm39) |
|
probably benign |
Het |
Nr4a3 |
C |
A |
4: 48,051,756 (GRCm39) |
P170Q |
possibly damaging |
Het |
Ntrk2 |
A |
G |
13: 59,208,109 (GRCm39) |
M652V |
probably damaging |
Het |
Or10n7-ps1 |
A |
T |
9: 39,597,812 (GRCm39) |
*143K |
probably null |
Het |
Or5b95 |
G |
A |
19: 12,657,471 (GRCm39) |
|
probably benign |
Het |
Paxbp1 |
T |
C |
16: 90,832,815 (GRCm39) |
I325V |
possibly damaging |
Het |
Pcare |
T |
C |
17: 72,059,137 (GRCm39) |
H180R |
probably benign |
Het |
Pi4ka |
G |
T |
16: 17,114,807 (GRCm39) |
|
probably benign |
Het |
Pira13 |
A |
G |
7: 3,825,380 (GRCm39) |
S421P |
probably damaging |
Het |
Pou6f1 |
T |
A |
15: 100,489,742 (GRCm39) |
D74V |
probably damaging |
Het |
Prpsap2 |
C |
A |
11: 61,627,870 (GRCm39) |
R202L |
probably damaging |
Het |
Ptprn |
A |
T |
1: 75,228,407 (GRCm39) |
L890Q |
probably damaging |
Het |
Ramp1 |
C |
G |
1: 91,134,137 (GRCm39) |
P97A |
probably benign |
Het |
Rbp3 |
T |
A |
14: 33,678,486 (GRCm39) |
F811L |
possibly damaging |
Het |
Rnf213 |
C |
A |
11: 119,305,250 (GRCm39) |
L494M |
probably damaging |
Het |
Rpl4 |
A |
G |
9: 64,082,245 (GRCm39) |
N48S |
probably benign |
Het |
Rsbn1l |
A |
G |
5: 21,110,841 (GRCm39) |
V499A |
probably damaging |
Het |
Sacs |
A |
G |
14: 61,430,022 (GRCm39) |
T691A |
probably benign |
Het |
Sass6 |
T |
C |
3: 116,407,709 (GRCm39) |
V275A |
probably benign |
Het |
Sdcbp |
T |
C |
4: 6,393,661 (GRCm39) |
S259P |
probably benign |
Het |
Sephs2 |
A |
G |
7: 126,872,206 (GRCm39) |
F296L |
probably benign |
Het |
Slc12a4 |
C |
T |
8: 106,673,322 (GRCm39) |
|
probably null |
Het |
Snrk |
G |
A |
9: 121,989,597 (GRCm39) |
V314I |
probably benign |
Het |
Tas1r3 |
C |
T |
4: 155,947,600 (GRCm39) |
|
probably null |
Het |
Tle3 |
T |
A |
9: 61,320,195 (GRCm39) |
V560E |
probably damaging |
Het |
Trdmt1 |
A |
G |
2: 13,526,918 (GRCm39) |
Y144H |
probably benign |
Het |
Trim42 |
T |
C |
9: 97,245,100 (GRCm39) |
T567A |
probably benign |
Het |
Tsbp1 |
A |
C |
17: 34,678,973 (GRCm39) |
R228S |
possibly damaging |
Het |
Tuba4a |
T |
C |
1: 75,193,945 (GRCm39) |
D74G |
probably benign |
Het |
Ube3c |
G |
A |
5: 29,842,769 (GRCm39) |
|
probably null |
Het |
Vwa3a |
A |
G |
7: 120,375,311 (GRCm39) |
D375G |
probably benign |
Het |
Zfp729b |
A |
G |
13: 67,741,218 (GRCm39) |
M349T |
possibly damaging |
Het |
|
Other mutations in Rapgefl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01487:Rapgefl1
|
APN |
11 |
98,737,961 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03088:Rapgefl1
|
APN |
11 |
98,740,058 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03048:Rapgefl1
|
UTSW |
11 |
98,727,990 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1807:Rapgefl1
|
UTSW |
11 |
98,736,815 (GRCm39) |
critical splice donor site |
probably null |
|
R1862:Rapgefl1
|
UTSW |
11 |
98,733,035 (GRCm39) |
missense |
probably benign |
|
R4078:Rapgefl1
|
UTSW |
11 |
98,740,803 (GRCm39) |
missense |
probably benign |
0.34 |
R4079:Rapgefl1
|
UTSW |
11 |
98,740,803 (GRCm39) |
missense |
probably benign |
0.34 |
R4869:Rapgefl1
|
UTSW |
11 |
98,741,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R5994:Rapgefl1
|
UTSW |
11 |
98,740,986 (GRCm39) |
missense |
probably benign |
0.06 |
R6275:Rapgefl1
|
UTSW |
11 |
98,741,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R6930:Rapgefl1
|
UTSW |
11 |
98,737,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R7138:Rapgefl1
|
UTSW |
11 |
98,737,900 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7432:Rapgefl1
|
UTSW |
11 |
98,741,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Rapgefl1
|
UTSW |
11 |
98,736,960 (GRCm39) |
missense |
probably benign |
0.12 |
R7761:Rapgefl1
|
UTSW |
11 |
98,728,485 (GRCm39) |
missense |
probably benign |
0.05 |
R7775:Rapgefl1
|
UTSW |
11 |
98,741,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R7824:Rapgefl1
|
UTSW |
11 |
98,741,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R8018:Rapgefl1
|
UTSW |
11 |
98,731,166 (GRCm39) |
critical splice donor site |
probably null |
|
R8099:Rapgefl1
|
UTSW |
11 |
98,738,209 (GRCm39) |
missense |
probably damaging |
0.98 |
R8501:Rapgefl1
|
UTSW |
11 |
98,733,053 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1088:Rapgefl1
|
UTSW |
11 |
98,736,721 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Rapgefl1
|
UTSW |
11 |
98,736,807 (GRCm39) |
missense |
probably damaging |
0.99 |
|