Incidental Mutation 'R0308:Fhad1'
| ID |
24958 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Fhad1
|
| Ensembl Gene |
ENSMUSG00000051435 |
| Gene Name |
forkhead-associated phosphopeptide binding domain 1 |
| Synonyms |
2900090M10Rik |
| MMRRC Submission |
038518-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.060)
|
| Stock # |
R0308 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
141617749-141742393 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to G
at 141712904 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000101406
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000105779]
[ENSMUST00000105780]
|
| AlphaFold |
A6PWD2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105779
|
| SMART Domains |
Protein: ENSMUSP00000101405
Gene: ENSMUSG00000051435
| Domain | Start | End | E-Value | Type |
|---|
|
FHA
|
17 |
69 |
8.41e-8 |
SMART |
|
low complexity region
|
111 |
124 |
N/A |
INTRINSIC |
|
coiled coil region
|
307 |
434 |
N/A |
INTRINSIC |
|
coiled coil region
|
640 |
915 |
N/A |
INTRINSIC |
|
low complexity region
|
1091 |
1102 |
N/A |
INTRINSIC |
|
coiled coil region
|
1111 |
1140 |
N/A |
INTRINSIC |
|
coiled coil region
|
1255 |
1339 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105780
|
| SMART Domains |
Protein: ENSMUSP00000101406
Gene: ENSMUSG00000051435
| Domain | Start | End | E-Value | Type |
|---|
|
FHA
|
17 |
69 |
8.41e-8 |
SMART |
|
low complexity region
|
111 |
124 |
N/A |
INTRINSIC |
|
coiled coil region
|
307 |
434 |
N/A |
INTRINSIC |
|
coiled coil region
|
640 |
915 |
N/A |
INTRINSIC |
|
low complexity region
|
1091 |
1102 |
N/A |
INTRINSIC |
|
coiled coil region
|
1111 |
1140 |
N/A |
INTRINSIC |
|
coiled coil region
|
1255 |
1339 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123068
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146094
|
| Coding Region Coverage |
- 1x: 98.8%
- 3x: 97.7%
- 10x: 95.1%
- 20x: 89.5%
|
| Validation Efficiency |
100% (82/82) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 81 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700009N14Rik |
A |
T |
4: 39,450,989 (GRCm39) |
D65V |
probably damaging |
Het |
| 4933407L21Rik |
A |
T |
1: 85,859,007 (GRCm39) |
|
probably benign |
Het |
| Abcc12 |
C |
T |
8: 87,284,381 (GRCm39) |
|
probably benign |
Het |
| Adamts12 |
A |
G |
15: 11,311,646 (GRCm39) |
E1301G |
probably damaging |
Het |
| Adh4 |
A |
T |
3: 138,129,863 (GRCm39) |
N230Y |
probably damaging |
Het |
| Anapc15-ps |
T |
A |
10: 95,508,954 (GRCm39) |
M109L |
probably benign |
Het |
| Angpt2 |
T |
C |
8: 18,742,141 (GRCm39) |
I472V |
possibly damaging |
Het |
| Arhgef26 |
C |
A |
3: 62,247,820 (GRCm39) |
D301E |
probably benign |
Het |
| Armc10 |
G |
A |
5: 21,852,295 (GRCm39) |
|
probably benign |
Het |
| Atm |
T |
C |
9: 53,365,773 (GRCm39) |
|
probably null |
Het |
| Atp5f1b |
T |
C |
10: 127,921,908 (GRCm39) |
V265A |
probably benign |
Het |
| Atp8b1 |
G |
T |
18: 64,678,315 (GRCm39) |
C860* |
probably null |
Het |
| Atrnl1 |
T |
G |
19: 57,741,720 (GRCm39) |
S1160A |
probably benign |
Het |
| Bmal1 |
A |
T |
7: 112,890,743 (GRCm39) |
I179F |
probably damaging |
Het |
| Cep55 |
A |
G |
19: 38,048,659 (GRCm39) |
E105G |
possibly damaging |
Het |
| Cfap54 |
C |
A |
10: 92,721,226 (GRCm39) |
D2502Y |
unknown |
Het |
| Cilp2 |
A |
G |
8: 70,335,643 (GRCm39) |
S452P |
probably benign |
Het |
| Clptm1l |
A |
G |
13: 73,759,786 (GRCm39) |
D282G |
possibly damaging |
Het |
| Csrp1 |
C |
A |
1: 135,673,024 (GRCm39) |
T47N |
probably damaging |
Het |
| Cyp2c40 |
T |
A |
19: 39,766,432 (GRCm39) |
I388F |
probably damaging |
Het |
| Dars1 |
C |
T |
1: 128,291,996 (GRCm39) |
R494H |
probably damaging |
Het |
| Dna2 |
T |
C |
10: 62,792,753 (GRCm39) |
V256A |
probably damaging |
Het |
| Dock7 |
T |
C |
4: 98,873,051 (GRCm39) |
T1132A |
probably benign |
Het |
| Dpcd |
T |
G |
19: 45,565,445 (GRCm39) |
F140V |
probably damaging |
Het |
| Elk3 |
A |
T |
10: 93,101,067 (GRCm39) |
M228K |
probably benign |
Het |
| Erich6 |
A |
G |
3: 58,543,525 (GRCm39) |
F182L |
probably damaging |
Het |
| Fryl |
A |
T |
5: 73,198,947 (GRCm39) |
|
probably benign |
Het |
| Fzd9 |
A |
T |
5: 135,278,260 (GRCm39) |
C542S |
probably damaging |
Het |
| Gba1 |
A |
G |
3: 89,115,671 (GRCm39) |
T460A |
probably benign |
Het |
| Gli2 |
C |
T |
1: 118,769,792 (GRCm39) |
A587T |
probably benign |
Het |
| Gm11011 |
C |
T |
2: 169,424,614 (GRCm39) |
|
probably benign |
Het |
| Gmppb |
A |
G |
9: 107,927,033 (GRCm39) |
E68G |
probably benign |
Het |
| Gpld1 |
A |
G |
13: 25,146,818 (GRCm39) |
N260S |
possibly damaging |
Het |
| Hipk3 |
G |
A |
2: 104,263,552 (GRCm39) |
S900L |
probably damaging |
Het |
| Idi2l |
T |
G |
13: 8,990,877 (GRCm39) |
|
probably benign |
Het |
| Ints6l |
A |
T |
X: 55,526,715 (GRCm39) |
M215L |
possibly damaging |
Het |
| Irx6 |
T |
A |
8: 93,403,659 (GRCm39) |
L128Q |
probably damaging |
Het |
| Itga10 |
T |
C |
3: 96,558,780 (GRCm39) |
S373P |
probably damaging |
Het |
| Jak1 |
T |
C |
4: 101,011,732 (GRCm39) |
|
probably null |
Het |
| Jak2 |
C |
T |
19: 29,289,157 (GRCm39) |
T1103I |
probably benign |
Het |
| Katnal1 |
A |
T |
5: 148,815,734 (GRCm39) |
V401D |
possibly damaging |
Het |
| Krbox5 |
A |
G |
13: 67,991,232 (GRCm39) |
|
probably benign |
Het |
| Lrp2 |
T |
A |
2: 69,313,326 (GRCm39) |
|
probably benign |
Het |
| Map3k13 |
A |
G |
16: 21,710,738 (GRCm39) |
H7R |
probably benign |
Het |
| Mrgprx3-ps |
A |
G |
7: 46,959,766 (GRCm39) |
V75A |
probably benign |
Het |
| Nol6 |
C |
T |
4: 41,123,584 (GRCm39) |
A55T |
probably benign |
Het |
| Opa1 |
G |
A |
16: 29,440,349 (GRCm39) |
R818Q |
probably damaging |
Het |
| Opn4 |
T |
C |
14: 34,319,081 (GRCm39) |
Y168C |
possibly damaging |
Het |
| Or8b35 |
A |
G |
9: 37,904,141 (GRCm39) |
I118V |
probably benign |
Het |
| Phf21a |
T |
C |
2: 92,161,122 (GRCm39) |
V330A |
possibly damaging |
Het |
| Phykpl |
A |
G |
11: 51,484,423 (GRCm39) |
|
probably benign |
Het |
| Plcb1 |
T |
G |
2: 134,655,534 (GRCm39) |
V38G |
probably benign |
Het |
| Plxna4 |
T |
A |
6: 32,214,703 (GRCm39) |
T593S |
probably benign |
Het |
| Poll |
A |
T |
19: 45,544,404 (GRCm39) |
I339N |
probably damaging |
Het |
| Rev3l |
A |
G |
10: 39,700,890 (GRCm39) |
I1796V |
probably benign |
Het |
| Rnf103 |
G |
A |
6: 71,486,686 (GRCm39) |
R439H |
probably damaging |
Het |
| Rrn3 |
G |
A |
16: 13,617,746 (GRCm39) |
|
probably benign |
Het |
| Sec14l4 |
G |
A |
11: 3,991,726 (GRCm39) |
|
probably benign |
Het |
| Sec23a |
A |
C |
12: 59,053,985 (GRCm39) |
Y4* |
probably null |
Het |
| Senp6 |
T |
C |
9: 80,040,265 (GRCm39) |
|
probably null |
Het |
| Serpinb6b |
A |
T |
13: 33,162,220 (GRCm39) |
N221Y |
probably benign |
Het |
| Slc6a2 |
A |
G |
8: 93,687,988 (GRCm39) |
E38G |
possibly damaging |
Het |
| Smap1 |
A |
T |
1: 23,888,423 (GRCm39) |
L196I |
probably damaging |
Het |
| Sorbs2 |
C |
T |
8: 46,248,167 (GRCm39) |
Q473* |
probably null |
Het |
| Sphkap |
C |
A |
1: 83,254,690 (GRCm39) |
V1020F |
probably damaging |
Het |
| Srfbp1 |
T |
C |
18: 52,621,614 (GRCm39) |
V225A |
probably benign |
Het |
| Srprb |
G |
A |
9: 103,079,204 (GRCm39) |
P728S |
possibly damaging |
Het |
| Tarm1 |
T |
C |
7: 3,545,187 (GRCm39) |
|
probably benign |
Het |
| Tcp1 |
T |
A |
17: 13,139,306 (GRCm39) |
I162N |
probably benign |
Het |
| Tmem237 |
C |
A |
1: 59,146,676 (GRCm39) |
A292S |
probably damaging |
Het |
| Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
| Tnpo1 |
A |
G |
13: 98,983,011 (GRCm39) |
F884L |
probably damaging |
Het |
| Trim7 |
A |
G |
11: 48,740,328 (GRCm39) |
T142A |
probably damaging |
Het |
| Ttn |
T |
A |
2: 76,616,024 (GRCm39) |
I14894F |
probably damaging |
Het |
| Tubgcp6 |
T |
C |
15: 89,006,639 (GRCm39) |
R128G |
possibly damaging |
Het |
| Ube2d2b |
A |
G |
5: 107,978,774 (GRCm39) |
T142A |
possibly damaging |
Het |
| Unc13c |
G |
T |
9: 73,388,400 (GRCm39) |
L2129I |
probably benign |
Het |
| Ushbp1 |
T |
C |
8: 71,843,697 (GRCm39) |
D247G |
probably damaging |
Het |
| Usp43 |
G |
A |
11: 67,770,966 (GRCm39) |
A556V |
probably damaging |
Het |
| Zfp438 |
T |
A |
18: 5,213,638 (GRCm39) |
H440L |
probably benign |
Het |
| Zfp518b |
C |
T |
5: 38,830,113 (GRCm39) |
E631K |
possibly damaging |
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 |
|
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 |
|
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 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCCTTGGACACAGGACACAGAGAAG -3'
(R):5'- ATGTACACAGGAACGCACAGGC -3'
Sequencing Primer
(F):5'- GAGGTAACAAGTTCCCCCAGG -3'
(R):5'- ggtggtggtggtggtgg -3'
|
| Posted On |
2013-04-16 |
Incidental Mutation