Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
G |
A |
3: 59,843,830 (GRCm39) |
V175I |
probably benign |
Het |
Abcb1a |
A |
T |
5: 8,736,164 (GRCm39) |
I186F |
probably benign |
Het |
Afg3l1 |
T |
C |
8: 124,221,678 (GRCm39) |
|
probably benign |
Het |
Atg4a |
G |
A |
X: 139,893,589 (GRCm39) |
E106K |
probably benign |
Het |
Ccdc50 |
A |
G |
16: 27,225,479 (GRCm39) |
E64G |
probably damaging |
Het |
Celsr3 |
G |
T |
9: 108,706,507 (GRCm39) |
G997W |
probably damaging |
Het |
Chd8 |
C |
T |
14: 52,441,952 (GRCm39) |
E2138K |
possibly damaging |
Het |
Col19a1 |
C |
T |
1: 24,598,762 (GRCm39) |
G77E |
unknown |
Het |
Dnaaf11 |
A |
G |
15: 66,319,525 (GRCm39) |
|
probably benign |
Het |
Fzr1 |
G |
T |
10: 81,205,252 (GRCm39) |
T159K |
probably damaging |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably null |
Het |
Gna13 |
T |
C |
11: 109,253,951 (GRCm39) |
I51T |
probably damaging |
Het |
Gorab |
A |
G |
1: 163,224,375 (GRCm39) |
|
probably null |
Het |
Hydin |
T |
C |
8: 111,245,746 (GRCm39) |
V2153A |
probably benign |
Het |
Ints6 |
A |
G |
14: 62,942,275 (GRCm39) |
V486A |
probably damaging |
Het |
Irx2 |
A |
G |
13: 72,779,709 (GRCm39) |
K331R |
probably damaging |
Het |
Mark2 |
T |
C |
19: 7,264,227 (GRCm39) |
E116G |
probably damaging |
Het |
Med14 |
A |
T |
X: 12,550,235 (GRCm39) |
H684Q |
probably benign |
Het |
Or1e25 |
A |
T |
11: 73,494,209 (GRCm39) |
T268S |
probably benign |
Het |
Pde5a |
T |
C |
3: 122,645,357 (GRCm39) |
L755P |
probably damaging |
Het |
Pex14 |
A |
T |
4: 149,047,968 (GRCm39) |
I203N |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,168,657 (GRCm39) |
E691G |
probably damaging |
Het |
Plekha1 |
G |
T |
7: 130,510,095 (GRCm39) |
W280C |
probably damaging |
Het |
Pnoc |
A |
T |
14: 65,642,284 (GRCm39) |
F160I |
probably damaging |
Het |
Ppfia3 |
C |
A |
7: 45,005,852 (GRCm39) |
R348L |
probably damaging |
Het |
Ppil6 |
A |
T |
10: 41,377,689 (GRCm39) |
|
probably benign |
Het |
Psmd13 |
C |
A |
7: 140,477,653 (GRCm39) |
|
probably benign |
Het |
Psme4 |
T |
C |
11: 30,795,173 (GRCm39) |
|
probably benign |
Het |
Rfx3 |
T |
C |
19: 27,784,186 (GRCm39) |
|
probably benign |
Het |
Rnase11 |
A |
G |
14: 51,287,227 (GRCm39) |
L109S |
probably damaging |
Het |
Rngtt |
A |
G |
4: 33,368,678 (GRCm39) |
T404A |
probably benign |
Het |
Sbf1 |
A |
G |
15: 89,187,421 (GRCm39) |
|
probably null |
Het |
Sema5b |
A |
G |
16: 35,480,301 (GRCm39) |
N656S |
probably damaging |
Het |
Ssh3 |
T |
C |
19: 4,315,324 (GRCm39) |
Y338C |
probably damaging |
Het |
Tgfbr3l |
A |
G |
8: 4,299,280 (GRCm39) |
D49G |
probably damaging |
Het |
Thbs1 |
C |
T |
2: 117,948,109 (GRCm39) |
T423I |
probably benign |
Het |
Ttc17 |
A |
T |
2: 94,206,419 (GRCm39) |
Y243* |
probably null |
Het |
Zbtb8os |
A |
T |
4: 129,235,309 (GRCm39) |
E54D |
probably damaging |
Het |
Zfp648 |
A |
T |
1: 154,080,881 (GRCm39) |
K347* |
probably null |
Het |
Zfp84 |
T |
G |
7: 29,474,758 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Fhad1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Fhad1
|
APN |
4 |
141,632,923 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01478:Fhad1
|
APN |
4 |
141,678,949 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01752:Fhad1
|
APN |
4 |
141,700,210 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01788:Fhad1
|
APN |
4 |
141,660,113 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01919:Fhad1
|
APN |
4 |
141,691,906 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02489:Fhad1
|
APN |
4 |
141,684,931 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02568:Fhad1
|
APN |
4 |
141,660,105 (GRCm39) |
missense |
probably null |
1.00 |
IGL02583:Fhad1
|
APN |
4 |
141,738,955 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02716:Fhad1
|
APN |
4 |
141,645,642 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02819:Fhad1
|
APN |
4 |
141,646,069 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02820:Fhad1
|
APN |
4 |
141,646,069 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03038:Fhad1
|
APN |
4 |
141,729,805 (GRCm39) |
missense |
probably benign |
0.38 |
IGL03167:Fhad1
|
APN |
4 |
141,700,108 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03255:Fhad1
|
APN |
4 |
141,700,191 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4466_Fhad1_343
|
UTSW |
4 |
141,684,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831_Fhad1_494
|
UTSW |
4 |
141,643,378 (GRCm39) |
splice site |
probably null |
|
R5504_Fhad1_818
|
UTSW |
4 |
141,712,846 (GRCm39) |
missense |
probably benign |
|
BB002:Fhad1
|
UTSW |
4 |
141,681,498 (GRCm39) |
missense |
probably damaging |
0.97 |
BB012:Fhad1
|
UTSW |
4 |
141,681,498 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT1430001:Fhad1
|
UTSW |
4 |
141,637,060 (GRCm39) |
missense |
probably damaging |
0.99 |
R0014:Fhad1
|
UTSW |
4 |
141,655,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Fhad1
|
UTSW |
4 |
141,667,406 (GRCm39) |
missense |
probably benign |
0.06 |
R0143:Fhad1
|
UTSW |
4 |
141,656,957 (GRCm39) |
splice site |
probably benign |
|
R0178:Fhad1
|
UTSW |
4 |
141,682,651 (GRCm39) |
missense |
probably benign |
0.31 |
R0308:Fhad1
|
UTSW |
4 |
141,712,904 (GRCm39) |
splice site |
probably benign |
|
R0384:Fhad1
|
UTSW |
4 |
141,729,737 (GRCm39) |
missense |
probably benign |
|
R0583:Fhad1
|
UTSW |
4 |
141,631,301 (GRCm39) |
missense |
probably benign |
0.37 |
R1501:Fhad1
|
UTSW |
4 |
141,691,936 (GRCm39) |
missense |
probably benign |
|
R1584:Fhad1
|
UTSW |
4 |
141,712,822 (GRCm39) |
missense |
probably benign |
0.22 |
R1615:Fhad1
|
UTSW |
4 |
141,649,634 (GRCm39) |
missense |
probably damaging |
0.99 |
R1991:Fhad1
|
UTSW |
4 |
141,709,473 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2060:Fhad1
|
UTSW |
4 |
141,626,560 (GRCm39) |
missense |
probably benign |
0.08 |
R2079:Fhad1
|
UTSW |
4 |
141,718,513 (GRCm39) |
nonsense |
probably null |
|
R2133:Fhad1
|
UTSW |
4 |
141,655,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R2337:Fhad1
|
UTSW |
4 |
141,649,655 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2843:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2845:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2846:Fhad1
|
UTSW |
4 |
141,632,279 (GRCm39) |
missense |
probably benign |
0.06 |
R2866:Fhad1
|
UTSW |
4 |
141,648,099 (GRCm39) |
missense |
probably benign |
0.00 |
R3119:Fhad1
|
UTSW |
4 |
141,645,618 (GRCm39) |
frame shift |
probably null |
|
R3760:Fhad1
|
UTSW |
4 |
141,637,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R4180:Fhad1
|
UTSW |
4 |
141,712,854 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4466:Fhad1
|
UTSW |
4 |
141,684,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Fhad1
|
UTSW |
4 |
141,623,779 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4680:Fhad1
|
UTSW |
4 |
141,738,858 (GRCm39) |
nonsense |
probably null |
|
R4725:Fhad1
|
UTSW |
4 |
141,655,689 (GRCm39) |
critical splice donor site |
probably null |
|
R4755:Fhad1
|
UTSW |
4 |
141,655,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Fhad1
|
UTSW |
4 |
141,643,378 (GRCm39) |
splice site |
probably null |
|
R4909:Fhad1
|
UTSW |
4 |
141,712,822 (GRCm39) |
missense |
probably benign |
0.01 |
R4968:Fhad1
|
UTSW |
4 |
141,645,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Fhad1
|
UTSW |
4 |
141,729,910 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5036:Fhad1
|
UTSW |
4 |
141,648,052 (GRCm39) |
missense |
probably benign |
0.03 |
R5048:Fhad1
|
UTSW |
4 |
141,691,987 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5416:Fhad1
|
UTSW |
4 |
141,646,113 (GRCm39) |
missense |
probably benign |
0.39 |
R5504:Fhad1
|
UTSW |
4 |
141,712,846 (GRCm39) |
missense |
probably benign |
|
R5586:Fhad1
|
UTSW |
4 |
141,632,442 (GRCm39) |
missense |
probably benign |
0.44 |
R5692:Fhad1
|
UTSW |
4 |
141,690,768 (GRCm39) |
missense |
probably benign |
0.00 |
R5706:Fhad1
|
UTSW |
4 |
141,681,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Fhad1
|
UTSW |
4 |
141,656,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R5823:Fhad1
|
UTSW |
4 |
141,682,617 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5833:Fhad1
|
UTSW |
4 |
141,729,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Fhad1
|
UTSW |
4 |
141,618,263 (GRCm39) |
nonsense |
probably null |
|
R6286:Fhad1
|
UTSW |
4 |
141,648,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R6610:Fhad1
|
UTSW |
4 |
141,643,707 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6755:Fhad1
|
UTSW |
4 |
141,691,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7006:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7008:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7012:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7014:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7058:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7059:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7060:Fhad1
|
UTSW |
4 |
141,645,602 (GRCm39) |
frame shift |
probably null |
|
R7159:Fhad1
|
UTSW |
4 |
141,678,927 (GRCm39) |
missense |
probably benign |
0.01 |
R7472:Fhad1
|
UTSW |
4 |
141,691,937 (GRCm39) |
missense |
probably benign |
|
R7670:Fhad1
|
UTSW |
4 |
141,678,802 (GRCm39) |
missense |
probably benign |
0.01 |
R7694:Fhad1
|
UTSW |
4 |
141,632,375 (GRCm39) |
missense |
probably benign |
0.41 |
R7745:Fhad1
|
UTSW |
4 |
141,618,250 (GRCm39) |
missense |
probably benign |
0.00 |
R7848:Fhad1
|
UTSW |
4 |
141,632,913 (GRCm39) |
missense |
probably benign |
0.29 |
R7853:Fhad1
|
UTSW |
4 |
141,637,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R7867:Fhad1
|
UTSW |
4 |
141,632,902 (GRCm39) |
missense |
probably benign |
0.00 |
R7925:Fhad1
|
UTSW |
4 |
141,681,498 (GRCm39) |
missense |
probably damaging |
0.97 |
R8089:Fhad1
|
UTSW |
4 |
141,684,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8123:Fhad1
|
UTSW |
4 |
141,712,836 (GRCm39) |
missense |
probably benign |
0.02 |
R8711:Fhad1
|
UTSW |
4 |
141,684,924 (GRCm39) |
missense |
probably benign |
0.25 |
R8751:Fhad1
|
UTSW |
4 |
141,646,134 (GRCm39) |
missense |
probably benign |
0.04 |
R8783:Fhad1
|
UTSW |
4 |
141,636,403 (GRCm39) |
missense |
probably benign |
0.02 |
R8858:Fhad1
|
UTSW |
4 |
141,666,339 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8867:Fhad1
|
UTSW |
4 |
141,656,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R8890:Fhad1
|
UTSW |
4 |
141,656,902 (GRCm39) |
missense |
probably benign |
0.01 |
R8982:Fhad1
|
UTSW |
4 |
141,729,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Fhad1
|
UTSW |
4 |
141,649,735 (GRCm39) |
splice site |
probably benign |
|
R9021:Fhad1
|
UTSW |
4 |
141,709,620 (GRCm39) |
missense |
probably damaging |
0.97 |
R9190:Fhad1
|
UTSW |
4 |
141,646,058 (GRCm39) |
critical splice donor site |
probably null |
|
R9237:Fhad1
|
UTSW |
4 |
141,632,483 (GRCm39) |
missense |
probably benign |
0.11 |
R9614:Fhad1
|
UTSW |
4 |
141,678,882 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9744:Fhad1
|
UTSW |
4 |
141,637,124 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Fhad1
|
UTSW |
4 |
141,678,927 (GRCm39) |
missense |
probably benign |
0.01 |
|