Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
A |
T |
8: 60,969,106 (GRCm39) |
D117V |
probably damaging |
Het |
Abca14 |
T |
C |
7: 119,852,644 (GRCm39) |
Y870H |
possibly damaging |
Het |
Ankrd36 |
T |
C |
11: 5,585,092 (GRCm39) |
I301T |
probably benign |
Het |
Atp10b |
T |
A |
11: 43,150,672 (GRCm39) |
S1457T |
probably benign |
Het |
Bltp1 |
A |
G |
3: 36,996,531 (GRCm39) |
D1081G |
possibly damaging |
Het |
Ccdc175 |
G |
A |
12: 72,177,916 (GRCm39) |
|
probably benign |
Het |
Ccdc93 |
A |
G |
1: 121,389,628 (GRCm39) |
K224E |
probably benign |
Het |
Cep131 |
C |
T |
11: 119,956,786 (GRCm39) |
A886T |
probably damaging |
Het |
Clip1 |
A |
C |
5: 123,717,442 (GRCm39) |
H1282Q |
probably damaging |
Het |
Ctcfl |
T |
G |
2: 172,959,177 (GRCm39) |
D183A |
probably benign |
Het |
Cyp17a1 |
C |
T |
19: 46,659,495 (GRCm39) |
V112I |
probably benign |
Het |
Gipc2 |
A |
G |
3: 151,843,214 (GRCm39) |
I141T |
probably damaging |
Het |
Glo1 |
T |
C |
17: 30,815,393 (GRCm39) |
R141G |
possibly damaging |
Het |
Ipmk |
C |
A |
10: 71,208,631 (GRCm39) |
A140E |
probably damaging |
Het |
Kynu |
A |
G |
2: 43,561,394 (GRCm39) |
D310G |
possibly damaging |
Het |
Myo1f |
T |
A |
17: 33,798,857 (GRCm39) |
I174N |
probably damaging |
Het |
Nat10 |
T |
A |
2: 103,588,102 (GRCm39) |
N8Y |
probably damaging |
Het |
Nhlrc2 |
A |
G |
19: 56,564,587 (GRCm39) |
I304V |
probably benign |
Het |
Pdk4 |
T |
C |
6: 5,491,979 (GRCm39) |
H31R |
probably damaging |
Het |
Sema6d |
T |
C |
2: 124,505,995 (GRCm39) |
V644A |
possibly damaging |
Het |
Slc30a4 |
T |
A |
2: 122,544,308 (GRCm39) |
K11N |
possibly damaging |
Het |
Slc6a3 |
T |
C |
13: 73,686,668 (GRCm39) |
S12P |
probably benign |
Het |
Spats2 |
C |
T |
15: 99,110,127 (GRCm39) |
A508V |
probably benign |
Het |
Tinag |
A |
G |
9: 76,952,820 (GRCm39) |
Y55H |
probably damaging |
Het |
Topbp1 |
T |
C |
9: 103,188,844 (GRCm39) |
I172T |
possibly damaging |
Het |
Trim17 |
A |
G |
11: 58,861,423 (GRCm39) |
T279A |
probably damaging |
Het |
Vmn1r216 |
C |
A |
13: 23,283,519 (GRCm39) |
N67K |
probably benign |
Het |
Washc4 |
T |
C |
10: 83,411,996 (GRCm39) |
L709P |
probably benign |
Het |
Xdh |
T |
C |
17: 74,230,132 (GRCm39) |
|
probably null |
Het |
Zfhx4 |
C |
T |
3: 5,309,036 (GRCm39) |
P754L |
probably damaging |
Het |
Zfp267 |
T |
C |
3: 36,218,729 (GRCm39) |
Y251H |
possibly damaging |
Het |
Zfp623 |
C |
A |
15: 75,819,528 (GRCm39) |
S161R |
probably benign |
Het |
Zmat3 |
G |
A |
3: 32,395,827 (GRCm39) |
R227C |
possibly damaging |
Het |
|
Other mutations in Fhod3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Fhod3
|
APN |
18 |
25,127,597 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01139:Fhod3
|
APN |
18 |
25,199,401 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01293:Fhod3
|
APN |
18 |
25,153,709 (GRCm39) |
splice site |
probably benign |
|
IGL01313:Fhod3
|
APN |
18 |
25,153,777 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01568:Fhod3
|
APN |
18 |
25,253,219 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01586:Fhod3
|
APN |
18 |
25,223,804 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01622:Fhod3
|
APN |
18 |
25,155,924 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01623:Fhod3
|
APN |
18 |
25,155,924 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01640:Fhod3
|
APN |
18 |
25,248,850 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01860:Fhod3
|
APN |
18 |
25,037,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01860:Fhod3
|
APN |
18 |
25,030,738 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02192:Fhod3
|
APN |
18 |
25,189,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02390:Fhod3
|
APN |
18 |
25,199,332 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02550:Fhod3
|
APN |
18 |
25,156,017 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02987:Fhod3
|
APN |
18 |
25,246,610 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0328:Fhod3
|
UTSW |
18 |
25,246,657 (GRCm39) |
missense |
probably benign |
0.01 |
R0362:Fhod3
|
UTSW |
18 |
25,223,133 (GRCm39) |
nonsense |
probably null |
|
R0373:Fhod3
|
UTSW |
18 |
25,223,161 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0483:Fhod3
|
UTSW |
18 |
24,842,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R0570:Fhod3
|
UTSW |
18 |
25,245,640 (GRCm39) |
missense |
probably benign |
0.27 |
R0617:Fhod3
|
UTSW |
18 |
25,245,736 (GRCm39) |
splice site |
probably benign |
|
R0834:Fhod3
|
UTSW |
18 |
25,248,862 (GRCm39) |
nonsense |
probably null |
|
R0836:Fhod3
|
UTSW |
18 |
25,199,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Fhod3
|
UTSW |
18 |
25,153,722 (GRCm39) |
small deletion |
probably benign |
|
R1157:Fhod3
|
UTSW |
18 |
25,118,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1158:Fhod3
|
UTSW |
18 |
25,118,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1160:Fhod3
|
UTSW |
18 |
25,118,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1381:Fhod3
|
UTSW |
18 |
25,223,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Fhod3
|
UTSW |
18 |
25,248,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R1621:Fhod3
|
UTSW |
18 |
25,155,924 (GRCm39) |
missense |
probably benign |
0.35 |
R1748:Fhod3
|
UTSW |
18 |
24,903,550 (GRCm39) |
nonsense |
probably null |
|
R1757:Fhod3
|
UTSW |
18 |
25,199,335 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1758:Fhod3
|
UTSW |
18 |
25,253,367 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1872:Fhod3
|
UTSW |
18 |
25,263,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Fhod3
|
UTSW |
18 |
25,245,643 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1917:Fhod3
|
UTSW |
18 |
25,218,658 (GRCm39) |
missense |
probably benign |
0.27 |
R1917:Fhod3
|
UTSW |
18 |
25,123,022 (GRCm39) |
splice site |
probably benign |
|
R1934:Fhod3
|
UTSW |
18 |
25,223,335 (GRCm39) |
missense |
probably benign |
0.35 |
R1958:Fhod3
|
UTSW |
18 |
25,223,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Fhod3
|
UTSW |
18 |
25,223,473 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3618:Fhod3
|
UTSW |
18 |
25,153,722 (GRCm39) |
small deletion |
probably benign |
|
R3709:Fhod3
|
UTSW |
18 |
25,223,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R3937:Fhod3
|
UTSW |
18 |
25,223,818 (GRCm39) |
missense |
probably benign |
0.44 |
R4246:Fhod3
|
UTSW |
18 |
25,123,123 (GRCm39) |
missense |
probably null |
1.00 |
R4248:Fhod3
|
UTSW |
18 |
25,123,123 (GRCm39) |
missense |
probably null |
1.00 |
R4249:Fhod3
|
UTSW |
18 |
25,123,123 (GRCm39) |
missense |
probably null |
1.00 |
R4497:Fhod3
|
UTSW |
18 |
25,243,296 (GRCm39) |
critical splice donor site |
probably null |
|
R4498:Fhod3
|
UTSW |
18 |
25,243,296 (GRCm39) |
critical splice donor site |
probably null |
|
R4532:Fhod3
|
UTSW |
18 |
25,243,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R4596:Fhod3
|
UTSW |
18 |
25,248,775 (GRCm39) |
missense |
probably benign |
0.01 |
R4628:Fhod3
|
UTSW |
18 |
25,253,186 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4667:Fhod3
|
UTSW |
18 |
25,199,395 (GRCm39) |
missense |
probably benign |
0.00 |
R4668:Fhod3
|
UTSW |
18 |
25,199,395 (GRCm39) |
missense |
probably benign |
0.00 |
R4734:Fhod3
|
UTSW |
18 |
25,161,192 (GRCm39) |
missense |
probably benign |
0.00 |
R4753:Fhod3
|
UTSW |
18 |
25,223,382 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4796:Fhod3
|
UTSW |
18 |
25,118,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Fhod3
|
UTSW |
18 |
25,223,305 (GRCm39) |
missense |
probably benign |
0.00 |
R5338:Fhod3
|
UTSW |
18 |
25,161,138 (GRCm39) |
missense |
probably damaging |
0.96 |
R5832:Fhod3
|
UTSW |
18 |
25,223,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R5863:Fhod3
|
UTSW |
18 |
25,258,810 (GRCm39) |
missense |
probably benign |
0.25 |
R6362:Fhod3
|
UTSW |
18 |
24,887,312 (GRCm39) |
missense |
probably benign |
0.00 |
R6414:Fhod3
|
UTSW |
18 |
25,223,935 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7099:Fhod3
|
UTSW |
18 |
25,223,219 (GRCm39) |
missense |
probably benign |
|
R7172:Fhod3
|
UTSW |
18 |
25,218,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Fhod3
|
UTSW |
18 |
25,223,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Fhod3
|
UTSW |
18 |
25,193,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R7294:Fhod3
|
UTSW |
18 |
25,266,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R7348:Fhod3
|
UTSW |
18 |
25,223,524 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7432:Fhod3
|
UTSW |
18 |
25,134,966 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7588:Fhod3
|
UTSW |
18 |
25,223,305 (GRCm39) |
missense |
probably benign |
0.02 |
R7629:Fhod3
|
UTSW |
18 |
24,887,374 (GRCm39) |
missense |
probably benign |
0.08 |
R7667:Fhod3
|
UTSW |
18 |
25,135,001 (GRCm39) |
missense |
probably benign |
|
R7681:Fhod3
|
UTSW |
18 |
25,123,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R7829:Fhod3
|
UTSW |
18 |
25,248,947 (GRCm39) |
critical splice donor site |
probably null |
|
R7889:Fhod3
|
UTSW |
18 |
24,903,551 (GRCm39) |
missense |
probably damaging |
0.99 |
R8072:Fhod3
|
UTSW |
18 |
25,153,722 (GRCm39) |
small deletion |
probably benign |
|
R8117:Fhod3
|
UTSW |
18 |
25,248,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R8245:Fhod3
|
UTSW |
18 |
25,246,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Fhod3
|
UTSW |
18 |
25,265,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R8518:Fhod3
|
UTSW |
18 |
25,189,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R8845:Fhod3
|
UTSW |
18 |
25,265,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R8889:Fhod3
|
UTSW |
18 |
25,189,452 (GRCm39) |
critical splice donor site |
probably null |
|
R8892:Fhod3
|
UTSW |
18 |
25,189,452 (GRCm39) |
critical splice donor site |
probably null |
|
R9016:Fhod3
|
UTSW |
18 |
25,243,136 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9035:Fhod3
|
UTSW |
18 |
25,161,140 (GRCm39) |
missense |
probably benign |
0.03 |
R9063:Fhod3
|
UTSW |
18 |
25,153,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R9157:Fhod3
|
UTSW |
18 |
25,218,651 (GRCm39) |
missense |
probably damaging |
0.98 |
R9201:Fhod3
|
UTSW |
18 |
25,127,613 (GRCm39) |
nonsense |
probably null |
|
R9244:Fhod3
|
UTSW |
18 |
25,248,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R9268:Fhod3
|
UTSW |
18 |
24,842,832 (GRCm39) |
critical splice donor site |
probably null |
|
R9272:Fhod3
|
UTSW |
18 |
25,030,681 (GRCm39) |
splice site |
probably benign |
|
R9415:Fhod3
|
UTSW |
18 |
25,102,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R9530:Fhod3
|
UTSW |
18 |
25,248,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R9596:Fhod3
|
UTSW |
18 |
25,193,392 (GRCm39) |
nonsense |
probably null |
|
R9739:Fhod3
|
UTSW |
18 |
24,903,566 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fhod3
|
UTSW |
18 |
25,153,763 (GRCm39) |
missense |
probably damaging |
1.00 |
|