Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
T |
7: 119,993,710 (GRCm39) |
Y1310F |
probably benign |
Het |
Ankrd54 |
A |
G |
15: 78,942,185 (GRCm39) |
F148L |
probably damaging |
Het |
Bag4 |
C |
T |
8: 26,259,528 (GRCm39) |
D224N |
probably damaging |
Het |
Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
Camk2b |
A |
T |
11: 5,942,856 (GRCm39) |
H126Q |
probably damaging |
Het |
Camsap3 |
G |
T |
8: 3,654,186 (GRCm39) |
V608L |
probably damaging |
Het |
Camsap3 |
A |
T |
8: 3,658,742 (GRCm39) |
M796L |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,853,517 (GRCm39) |
D308G |
probably benign |
Het |
Cpsf1 |
T |
C |
15: 76,486,710 (GRCm39) |
I275M |
probably damaging |
Het |
Cuta |
A |
G |
17: 27,157,856 (GRCm39) |
|
probably null |
Het |
Dclk2 |
A |
G |
3: 86,699,374 (GRCm39) |
|
probably benign |
Het |
Dst |
T |
G |
1: 34,289,761 (GRCm39) |
L784R |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,184,750 (GRCm39) |
M1681V |
possibly damaging |
Het |
Fbxo9 |
A |
T |
9: 77,994,494 (GRCm39) |
D274E |
probably damaging |
Het |
Frem2 |
T |
A |
3: 53,457,205 (GRCm39) |
D2049V |
probably damaging |
Het |
Fscn3 |
T |
C |
6: 28,430,174 (GRCm39) |
Y115H |
probably damaging |
Het |
Glp2r |
G |
T |
11: 67,655,603 (GRCm39) |
D46E |
probably benign |
Het |
Gpat2 |
G |
C |
2: 127,273,838 (GRCm39) |
G294R |
possibly damaging |
Het |
Irx5 |
A |
G |
8: 93,086,247 (GRCm39) |
Y110C |
probably damaging |
Het |
Kdm5d |
T |
C |
Y: 939,829 (GRCm39) |
S994P |
probably benign |
Homo |
Klhl2 |
A |
T |
8: 65,196,077 (GRCm39) |
C555* |
probably null |
Het |
Krtap4-7 |
A |
T |
11: 99,534,560 (GRCm39) |
I101N |
unknown |
Het |
Or13a27 |
A |
G |
7: 139,925,560 (GRCm39) |
L114P |
probably damaging |
Het |
Or4f57 |
A |
T |
2: 111,790,515 (GRCm39) |
V301E |
possibly damaging |
Het |
Pcdhb21 |
T |
C |
18: 37,648,961 (GRCm39) |
S697P |
probably damaging |
Het |
Pramel27 |
T |
C |
4: 143,579,326 (GRCm39) |
C304R |
probably damaging |
Het |
Rasgrf2 |
A |
T |
13: 92,167,361 (GRCm39) |
H237Q |
probably damaging |
Het |
Rnf216 |
A |
T |
5: 143,076,412 (GRCm39) |
D157E |
probably benign |
Het |
Rxrg |
T |
A |
1: 167,454,905 (GRCm39) |
F163I |
probably damaging |
Het |
Soat2 |
T |
A |
15: 102,069,028 (GRCm39) |
I351N |
probably damaging |
Het |
Srp72 |
C |
T |
5: 77,132,047 (GRCm39) |
T242I |
probably benign |
Het |
Svopl |
T |
C |
6: 38,018,002 (GRCm39) |
|
probably null |
Het |
Tbc1d2b |
G |
A |
9: 90,108,145 (GRCm39) |
P469S |
probably benign |
Het |
Tbkbp1 |
G |
A |
11: 97,029,578 (GRCm39) |
|
probably benign |
Het |
Tecta |
A |
G |
9: 42,295,523 (GRCm39) |
V324A |
probably damaging |
Het |
Twnk |
T |
C |
19: 44,998,931 (GRCm39) |
V557A |
probably damaging |
Het |
Vmn2r18 |
G |
A |
5: 151,485,889 (GRCm39) |
T535I |
probably damaging |
Het |
Zc3h14 |
T |
A |
12: 98,723,285 (GRCm39) |
S85T |
probably damaging |
Het |
|
Other mutations in Cfap299 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00775:Cfap299
|
APN |
5 |
98,932,369 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01133:Cfap299
|
APN |
5 |
98,646,240 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02151:Cfap299
|
APN |
5 |
98,477,301 (GRCm39) |
missense |
probably damaging |
1.00 |
LCD18:Cfap299
|
UTSW |
5 |
98,855,367 (GRCm39) |
intron |
probably benign |
|
PIT4514001:Cfap299
|
UTSW |
5 |
98,949,730 (GRCm39) |
missense |
probably benign |
0.00 |
R0962:Cfap299
|
UTSW |
5 |
98,714,420 (GRCm39) |
intron |
probably benign |
|
R1545:Cfap299
|
UTSW |
5 |
98,477,291 (GRCm39) |
missense |
probably benign |
0.25 |
R1886:Cfap299
|
UTSW |
5 |
98,949,690 (GRCm39) |
missense |
probably benign |
0.41 |
R1954:Cfap299
|
UTSW |
5 |
98,714,612 (GRCm39) |
intron |
probably benign |
|
R1965:Cfap299
|
UTSW |
5 |
98,494,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R2008:Cfap299
|
UTSW |
5 |
98,885,561 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3873:Cfap299
|
UTSW |
5 |
98,885,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4940:Cfap299
|
UTSW |
5 |
98,885,495 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5708:Cfap299
|
UTSW |
5 |
98,885,566 (GRCm39) |
missense |
probably benign |
|
R6509:Cfap299
|
UTSW |
5 |
98,477,256 (GRCm39) |
missense |
probably benign |
0.16 |
R7009:Cfap299
|
UTSW |
5 |
98,932,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R7911:Cfap299
|
UTSW |
5 |
98,885,567 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8211:Cfap299
|
UTSW |
5 |
98,477,294 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8317:Cfap299
|
UTSW |
5 |
98,885,459 (GRCm39) |
missense |
probably benign |
0.21 |
R9058:Cfap299
|
UTSW |
5 |
98,932,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R9293:Cfap299
|
UTSW |
5 |
98,646,162 (GRCm39) |
missense |
probably benign |
0.13 |
R9505:Cfap299
|
UTSW |
5 |
98,477,213 (GRCm39) |
start codon destroyed |
probably null |
0.21 |
R9681:Cfap299
|
UTSW |
5 |
98,477,214 (GRCm39) |
start codon destroyed |
probably null |
0.65 |
Z1177:Cfap299
|
UTSW |
5 |
98,949,693 (GRCm39) |
missense |
probably damaging |
1.00 |
|