Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaas |
C |
T |
15: 102,247,641 (GRCm39) |
R410H |
probably damaging |
Het |
Abca2 |
T |
C |
2: 25,332,370 (GRCm39) |
C1468R |
probably benign |
Het |
Actl9 |
T |
A |
17: 33,652,231 (GRCm39) |
I97N |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Asb3 |
T |
A |
11: 31,006,217 (GRCm39) |
M234K |
probably benign |
Het |
Bax |
A |
C |
7: 45,111,357 (GRCm39) |
H168Q |
probably null |
Het |
Brinp1 |
A |
G |
4: 68,681,192 (GRCm39) |
L446P |
possibly damaging |
Het |
Cdc14a |
A |
G |
3: 116,087,373 (GRCm39) |
|
probably null |
Het |
Cpq |
A |
T |
15: 33,250,146 (GRCm39) |
I168F |
probably damaging |
Het |
Crkl |
A |
T |
16: 17,301,556 (GRCm39) |
N270I |
probably damaging |
Het |
Cul7 |
G |
A |
17: 46,962,479 (GRCm39) |
E37K |
probably damaging |
Het |
Eps15 |
C |
T |
4: 109,169,526 (GRCm39) |
T112I |
probably benign |
Het |
F5 |
C |
T |
1: 164,036,529 (GRCm39) |
R1897* |
probably null |
Het |
Fbxl5 |
A |
T |
5: 43,928,140 (GRCm39) |
L40Q |
probably damaging |
Het |
Fhip1a |
C |
T |
3: 85,573,261 (GRCm39) |
S896N |
probably damaging |
Het |
Gprc5a |
C |
A |
6: 135,060,459 (GRCm39) |
T316K |
probably damaging |
Het |
Hectd4 |
T |
A |
5: 121,462,019 (GRCm39) |
L2299Q |
possibly damaging |
Het |
Khdc3 |
C |
G |
9: 73,010,942 (GRCm39) |
P240R |
probably benign |
Het |
Kif20b |
A |
G |
19: 34,906,318 (GRCm39) |
T69A |
probably damaging |
Het |
Kptn |
C |
G |
7: 15,857,888 (GRCm39) |
Q239E |
probably benign |
Het |
Lep |
T |
C |
6: 29,070,831 (GRCm39) |
S52P |
probably damaging |
Het |
Lrig3 |
G |
A |
10: 125,844,416 (GRCm39) |
V627M |
possibly damaging |
Het |
Lrrc37 |
T |
C |
11: 103,499,745 (GRCm39) |
K615E |
probably benign |
Het |
Mdga1 |
G |
A |
17: 30,061,876 (GRCm39) |
R792C |
probably damaging |
Het |
Mink1 |
T |
C |
11: 70,489,717 (GRCm39) |
V58A |
possibly damaging |
Het |
Neu1 |
G |
A |
17: 35,153,374 (GRCm39) |
R299Q |
probably benign |
Het |
Nrg3 |
T |
A |
14: 38,129,111 (GRCm39) |
I375F |
probably benign |
Het |
Nup50 |
A |
G |
15: 84,823,993 (GRCm39) |
T449A |
possibly damaging |
Het |
Nup98 |
A |
G |
7: 101,784,087 (GRCm39) |
S1082P |
possibly damaging |
Het |
Or8b1b |
C |
A |
9: 38,375,815 (GRCm39) |
H159Q |
probably benign |
Het |
Otub1 |
T |
C |
19: 7,176,571 (GRCm39) |
I188V |
probably benign |
Het |
Pcdhac2 |
T |
C |
18: 37,279,186 (GRCm39) |
I722T |
possibly damaging |
Het |
Pcsk7 |
T |
A |
9: 45,825,646 (GRCm39) |
D292E |
probably damaging |
Het |
Peli2 |
T |
A |
14: 48,490,174 (GRCm39) |
D215E |
probably benign |
Het |
Ppp1r9a |
T |
C |
6: 5,156,242 (GRCm39) |
|
probably null |
Het |
Ppp2r1b |
A |
G |
9: 50,773,725 (GRCm39) |
K136R |
possibly damaging |
Het |
Prpf3 |
T |
C |
3: 95,755,115 (GRCm39) |
K157E |
probably damaging |
Het |
Prss50 |
T |
C |
9: 110,690,336 (GRCm39) |
S160P |
probably damaging |
Het |
Ptprb |
T |
C |
10: 116,216,774 (GRCm39) |
V2251A |
probably damaging |
Het |
Rgs6 |
G |
A |
12: 83,162,951 (GRCm39) |
E386K |
probably damaging |
Het |
Rida |
A |
G |
15: 34,495,250 (GRCm39) |
I5T |
probably benign |
Het |
Rpe |
A |
G |
1: 66,740,169 (GRCm39) |
H35R |
probably damaging |
Het |
Sema4b |
T |
A |
7: 79,868,771 (GRCm39) |
D321E |
probably benign |
Het |
Slc22a13 |
G |
A |
9: 119,038,113 (GRCm39) |
A5V |
probably benign |
Het |
Snta1 |
C |
T |
2: 154,218,926 (GRCm39) |
|
probably null |
Het |
Spdye4c |
T |
A |
2: 128,437,632 (GRCm39) |
N220K |
probably benign |
Het |
Sult1c2 |
G |
T |
17: 54,269,176 (GRCm39) |
A280E |
possibly damaging |
Het |
Tfr2 |
A |
G |
5: 137,581,561 (GRCm39) |
E579G |
probably benign |
Het |
Tmem221 |
A |
G |
8: 72,011,182 (GRCm39) |
L91P |
probably damaging |
Het |
Tspear |
T |
A |
10: 77,706,253 (GRCm39) |
L341H |
possibly damaging |
Het |
Vmn1r17 |
A |
G |
6: 57,338,317 (GRCm39) |
V16A |
probably benign |
Het |
Vmn1r188 |
A |
G |
13: 22,272,603 (GRCm39) |
R186G |
probably damaging |
Het |
Wfikkn1 |
A |
G |
17: 26,097,565 (GRCm39) |
V253A |
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 |
|
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 |
R6595:Cfap299
|
UTSW |
5 |
98,949,717 (GRCm39) |
missense |
possibly damaging |
0.78 |
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 |
|