Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
A |
T |
11: 58,769,616 (GRCm39) |
K53* |
probably null |
Het |
4921513D11Rik |
T |
C |
17: 79,935,651 (GRCm39) |
S255P |
probably benign |
Het |
Ace |
A |
G |
11: 105,872,679 (GRCm39) |
N367S |
possibly damaging |
Het |
Agl |
A |
T |
3: 116,582,175 (GRCm39) |
N282K |
probably benign |
Het |
Ahnak |
C |
A |
19: 8,992,464 (GRCm39) |
P4583T |
probably damaging |
Het |
Alpi |
T |
C |
1: 87,029,247 (GRCm39) |
D4G |
probably benign |
Het |
Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
Aplnr |
T |
C |
2: 84,967,289 (GRCm39) |
Y105H |
probably damaging |
Het |
Arhgap9 |
G |
A |
10: 127,162,875 (GRCm39) |
R395K |
possibly damaging |
Het |
Asah1 |
A |
G |
8: 41,807,067 (GRCm39) |
M119T |
|
Het |
Atp5f1b |
T |
C |
10: 127,919,856 (GRCm39) |
F75L |
probably damaging |
Het |
B4galt6 |
G |
T |
18: 20,861,026 (GRCm39) |
N75K |
possibly damaging |
Het |
Bco1 |
A |
T |
8: 117,857,833 (GRCm39) |
H486L |
probably benign |
Het |
Btaf1 |
T |
A |
19: 36,947,351 (GRCm39) |
L480Q |
probably null |
Het |
Ccdc34 |
G |
T |
2: 109,871,078 (GRCm39) |
|
probably null |
Het |
Cdh19 |
T |
C |
1: 110,852,958 (GRCm39) |
S326G |
probably benign |
Het |
Cep89 |
A |
G |
7: 35,109,055 (GRCm39) |
D178G |
possibly damaging |
Het |
Cyp11b2 |
A |
T |
15: 74,725,854 (GRCm39) |
|
probably null |
Het |
Cyp21a1 |
A |
G |
17: 35,022,383 (GRCm39) |
I157T |
possibly damaging |
Het |
Dcbld2 |
A |
G |
16: 58,245,074 (GRCm39) |
D116G |
probably damaging |
Het |
Ddx5 |
T |
C |
11: 106,674,953 (GRCm39) |
Q377R |
probably damaging |
Het |
Deup1 |
T |
C |
9: 15,503,724 (GRCm39) |
D279G |
probably damaging |
Het |
F11 |
G |
A |
8: 45,698,770 (GRCm39) |
A458V |
probably benign |
Het |
Fhit |
C |
T |
14: 10,421,522 (GRCm38) |
V26M |
probably damaging |
Het |
Gjb5 |
A |
T |
4: 127,250,015 (GRCm39) |
V43E |
probably damaging |
Het |
Grtp1 |
A |
T |
8: 13,242,184 (GRCm39) |
I75N |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,533,221 (GRCm39) |
I3022T |
possibly damaging |
Het |
Hsp90ab1 |
T |
C |
17: 45,881,962 (GRCm39) |
T166A |
probably benign |
Het |
Ift70b |
T |
C |
2: 75,768,391 (GRCm39) |
I121V |
probably benign |
Het |
Iho1 |
C |
T |
9: 108,289,713 (GRCm39) |
V170M |
probably benign |
Het |
Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
Kcnk10 |
T |
C |
12: 98,401,161 (GRCm39) |
I491V |
probably benign |
Het |
Kcp |
A |
T |
6: 29,497,628 (GRCm39) |
C519* |
probably null |
Het |
Lcmt2 |
T |
C |
2: 120,970,217 (GRCm39) |
T69A |
probably benign |
Het |
Lmf1 |
A |
G |
17: 25,804,592 (GRCm39) |
Y90C |
probably damaging |
Het |
Lpp |
A |
G |
16: 24,798,064 (GRCm39) |
D612G |
probably damaging |
Het |
Lrfn5 |
C |
A |
12: 61,886,461 (GRCm39) |
S83Y |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 40,592,719 (GRCm39) |
|
probably null |
Het |
Lrp1b |
C |
T |
2: 41,679,074 (GRCm39) |
C6Y |
probably damaging |
Het |
Lrrc8c |
A |
G |
5: 105,754,993 (GRCm39) |
D256G |
probably damaging |
Het |
Mphosph10 |
A |
G |
7: 64,032,656 (GRCm39) |
Y478H |
probably damaging |
Het |
Mpp2 |
T |
C |
11: 101,955,124 (GRCm39) |
H167R |
probably benign |
Het |
Mtss1 |
A |
G |
15: 58,815,767 (GRCm39) |
S598P |
probably damaging |
Het |
Myh10 |
A |
G |
11: 68,684,049 (GRCm39) |
E1154G |
probably damaging |
Het |
Myo10 |
T |
C |
15: 25,808,270 (GRCm39) |
V1218A |
probably damaging |
Het |
Myo19 |
A |
G |
11: 84,792,328 (GRCm39) |
K599R |
probably damaging |
Het |
Neurl4 |
T |
C |
11: 69,798,134 (GRCm39) |
M771T |
probably damaging |
Het |
Nlrc4 |
A |
G |
17: 74,753,936 (GRCm39) |
V149A |
probably benign |
Het |
Nup133 |
A |
T |
8: 124,641,935 (GRCm39) |
S843T |
probably benign |
Het |
Or2y1c |
T |
C |
11: 49,361,358 (GRCm39) |
C127R |
probably damaging |
Het |
Or51k1 |
T |
C |
7: 103,661,777 (GRCm39) |
N44S |
probably damaging |
Het |
P3h2 |
A |
G |
16: 25,811,412 (GRCm39) |
|
probably null |
Het |
Piezo2 |
A |
T |
18: 63,278,042 (GRCm39) |
Y287* |
probably null |
Het |
Prob1 |
T |
C |
18: 35,785,605 (GRCm39) |
Y883C |
probably damaging |
Het |
Pxdn |
T |
A |
12: 30,050,011 (GRCm39) |
H506Q |
probably benign |
Het |
Ripor3 |
T |
C |
2: 167,827,037 (GRCm39) |
D658G |
probably benign |
Het |
Rufy1 |
T |
A |
11: 50,301,434 (GRCm39) |
I333L |
probably benign |
Het |
Selenok |
T |
A |
14: 29,692,064 (GRCm39) |
V34E |
probably benign |
Het |
Selplg |
T |
C |
5: 113,957,787 (GRCm39) |
E173G |
possibly damaging |
Het |
Septin10 |
A |
G |
10: 59,016,943 (GRCm39) |
F194L |
probably damaging |
Het |
Sptbn2 |
A |
T |
19: 4,779,230 (GRCm39) |
|
probably null |
Het |
St6galnac6 |
C |
T |
2: 32,498,098 (GRCm39) |
P6S |
probably benign |
Het |
Syngr2 |
T |
C |
11: 117,704,296 (GRCm39) |
Y194H |
probably damaging |
Het |
Thbs4 |
A |
G |
13: 92,894,576 (GRCm39) |
I649T |
possibly damaging |
Het |
Triobp |
T |
A |
15: 78,850,816 (GRCm39) |
N323K |
probably benign |
Het |
Tuba8 |
T |
A |
6: 121,197,548 (GRCm39) |
L70Q |
probably damaging |
Het |
Vmn2r61 |
A |
G |
7: 41,949,478 (GRCm39) |
T633A |
probably benign |
Het |
Zfp280b |
G |
T |
10: 75,875,188 (GRCm39) |
V356L |
probably damaging |
Het |
Zswim4 |
A |
T |
8: 84,944,001 (GRCm39) |
V746D |
probably benign |
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 |
R2844: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 |
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 |
|