Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
G |
A |
9: 55,880,991 (GRCm39) |
T146I |
unknown |
Het |
Abca16 |
A |
G |
7: 120,132,866 (GRCm39) |
E1265G |
probably benign |
Het |
Adar |
T |
C |
3: 89,654,882 (GRCm39) |
S924P |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,588,344 (GRCm39) |
V4414E |
possibly damaging |
Het |
AI429214 |
A |
T |
8: 37,460,820 (GRCm39) |
|
probably benign |
Het |
Ankmy1 |
A |
T |
1: 92,814,003 (GRCm39) |
L392Q |
probably benign |
Het |
Anxa3 |
A |
T |
5: 96,968,288 (GRCm39) |
I114F |
probably damaging |
Het |
Ccdc158 |
T |
C |
5: 92,771,260 (GRCm39) |
D985G |
possibly damaging |
Het |
Cndp2 |
C |
T |
18: 84,686,727 (GRCm39) |
V432I |
probably benign |
Het |
Ctbp2 |
T |
C |
7: 132,616,095 (GRCm39) |
K280R |
probably benign |
Het |
Dao |
AGG |
AG |
5: 114,153,270 (GRCm39) |
|
probably benign |
Het |
Dnaaf4 |
T |
A |
9: 72,879,598 (GRCm39) |
|
probably benign |
Het |
Dynap |
T |
C |
18: 70,375,093 (GRCm39) |
T41A |
possibly damaging |
Het |
Elfn2 |
A |
G |
15: 78,557,968 (GRCm39) |
L193P |
probably damaging |
Het |
Fcrl2 |
A |
T |
3: 87,166,933 (GRCm39) |
L20* |
probably null |
Het |
Flcn |
T |
C |
11: 59,684,948 (GRCm39) |
D501G |
probably damaging |
Het |
Gmip |
A |
G |
8: 70,268,143 (GRCm39) |
E399G |
probably benign |
Het |
Grm7 |
A |
G |
6: 111,184,737 (GRCm39) |
E356G |
probably benign |
Het |
Hs3st2 |
A |
G |
7: 121,099,639 (GRCm39) |
|
probably null |
Het |
Kcnh2 |
G |
A |
5: 24,525,014 (GRCm39) |
S1158L |
probably damaging |
Het |
Lancl2 |
A |
G |
6: 57,690,078 (GRCm39) |
T104A |
probably damaging |
Het |
Ldlrad4 |
G |
T |
18: 68,368,740 (GRCm39) |
A66S |
possibly damaging |
Het |
Mthfd2l |
T |
A |
5: 91,107,672 (GRCm39) |
I178N |
probably damaging |
Het |
Nbeal2 |
G |
T |
9: 110,458,225 (GRCm39) |
|
probably benign |
Het |
Niban1 |
A |
T |
1: 151,593,006 (GRCm39) |
K564* |
probably null |
Het |
Nipal3 |
C |
T |
4: 135,174,659 (GRCm39) |
R364H |
possibly damaging |
Het |
Or2b4 |
A |
G |
17: 38,116,038 (GRCm39) |
M1V |
probably null |
Het |
Oxa1l |
A |
G |
14: 54,600,757 (GRCm39) |
I77V |
not run |
Het |
Phf10 |
T |
A |
17: 15,174,378 (GRCm39) |
Q233H |
possibly damaging |
Het |
Pias2 |
T |
A |
18: 77,216,654 (GRCm39) |
N288K |
probably benign |
Het |
Pramel43 |
T |
C |
5: 94,761,839 (GRCm39) |
N244S |
probably benign |
Het |
Prm3 |
CTCTTCTTCTTCTTC |
CTCTTCTTCTTC |
16: 10,608,565 (GRCm39) |
|
probably benign |
Het |
Ptprd |
T |
C |
4: 76,003,757 (GRCm39) |
T1010A |
probably damaging |
Het |
Ralgapa2 |
T |
C |
2: 146,182,311 (GRCm39) |
D1676G |
probably damaging |
Het |
Rrp7a |
C |
T |
15: 83,001,125 (GRCm39) |
E269K |
possibly damaging |
Het |
Ryr3 |
A |
C |
2: 112,508,777 (GRCm39) |
M3399R |
probably damaging |
Het |
Secisbp2l |
C |
A |
2: 125,587,829 (GRCm39) |
R762L |
probably damaging |
Het |
Smad7 |
T |
G |
18: 75,502,355 (GRCm39) |
L110R |
possibly damaging |
Het |
St6gal1 |
G |
A |
16: 23,176,585 (GRCm39) |
A393T |
probably benign |
Het |
Tcea3 |
T |
G |
4: 135,985,229 (GRCm39) |
|
probably benign |
Het |
Tdrd9 |
T |
C |
12: 111,999,180 (GRCm39) |
V765A |
probably benign |
Het |
Tdrd9 |
C |
T |
12: 112,010,822 (GRCm39) |
R1130W |
probably damaging |
Het |
Tia1 |
C |
T |
6: 86,402,034 (GRCm39) |
P189S |
probably benign |
Het |
Tubg1 |
G |
T |
11: 101,014,854 (GRCm39) |
A199S |
probably benign |
Het |
Ubxn8 |
A |
G |
8: 34,113,243 (GRCm39) |
C204R |
probably damaging |
Het |
Vmn1r76 |
A |
G |
7: 11,664,810 (GRCm39) |
S135P |
probably damaging |
Het |
Vps18 |
T |
A |
2: 119,124,492 (GRCm39) |
L473H |
probably damaging |
Het |
Zfp444 |
A |
G |
7: 6,191,142 (GRCm39) |
T108A |
probably benign |
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 |
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 |
R8941:Rapgefl1
|
UTSW |
11 |
98,731,101 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|