Incidental Mutation 'R7472:Fhad1'
| ID |
581278 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Fhad1
|
| Ensembl Gene |
ENSMUSG00000051435 |
| Gene Name |
forkhead-associated phosphopeptide binding domain 1 |
| Synonyms |
2900090M10Rik |
| MMRRC Submission |
045546-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.057)
|
| Stock # |
R7472 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
141617749-141742393 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 141691937 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Cysteine
at position 400
(R400C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000101405
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000105779]
[ENSMUST00000105780]
|
| AlphaFold |
A6PWD2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105779
AA Change: R400C
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000101405
Gene: ENSMUSG00000051435
AA Change: R400C
| 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
AA Change: R400C
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000101406
Gene: ENSMUSG00000051435
AA Change: R400C
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.4%
|
| Validation Efficiency |
99% (99/100) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 99 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4921504E06Rik |
A |
G |
2: 19,545,219 (GRCm39) |
I78T |
probably benign |
Het |
| 4921524J17Rik |
G |
A |
8: 86,159,438 (GRCm39) |
|
probably benign |
Het |
| 4932438H23Rik |
T |
C |
16: 90,852,744 (GRCm39) |
T131A |
probably benign |
Het |
| Acbd6 |
G |
T |
1: 155,463,213 (GRCm39) |
E138* |
probably null |
Het |
| Ago3 |
A |
G |
4: 126,239,310 (GRCm39) |
V847A |
probably damaging |
Het |
| Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
| Als2cl |
C |
A |
9: 110,727,174 (GRCm39) |
H913Q |
probably benign |
Het |
| Atf6 |
A |
C |
1: 170,643,060 (GRCm39) |
S360R |
possibly damaging |
Het |
| Atm |
G |
C |
9: 53,359,425 (GRCm39) |
N2789K |
possibly damaging |
Het |
| Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
| Bpifa6 |
A |
T |
2: 153,831,249 (GRCm39) |
I272F |
possibly damaging |
Het |
| Cabin1 |
G |
T |
10: 75,494,481 (GRCm39) |
P1633T |
probably damaging |
Het |
| Camsap2 |
A |
G |
1: 136,209,131 (GRCm39) |
V119A |
probably damaging |
Het |
| Ccdc40 |
A |
G |
11: 119,153,974 (GRCm39) |
E1082G |
probably benign |
Het |
| Cchcr1 |
C |
A |
17: 35,839,248 (GRCm39) |
A479D |
probably damaging |
Het |
| Chpt1 |
C |
T |
10: 88,312,230 (GRCm39) |
V349I |
probably benign |
Het |
| Cldn13 |
A |
T |
5: 134,943,975 (GRCm39) |
I70K |
probably damaging |
Het |
| Col6a6 |
T |
A |
9: 105,659,622 (GRCm39) |
D441V |
probably damaging |
Het |
| Cpne5 |
G |
T |
17: 29,423,714 (GRCm39) |
T138K |
probably benign |
Het |
| Creb3l3 |
A |
T |
10: 80,925,301 (GRCm39) |
|
probably null |
Het |
| Cst5 |
C |
T |
2: 149,247,496 (GRCm39) |
L71F |
probably benign |
Het |
| Ctsb |
T |
C |
14: 63,375,550 (GRCm39) |
V172A |
probably benign |
Het |
| Cyp19a1 |
A |
G |
9: 54,074,277 (GRCm39) |
Y426H |
possibly damaging |
Het |
| Cyth4 |
T |
C |
15: 78,490,094 (GRCm39) |
F72S |
probably damaging |
Het |
| D430041D05Rik |
G |
T |
2: 104,240,484 (GRCm39) |
Q9K |
unknown |
Het |
| Dnah1 |
T |
A |
14: 30,983,547 (GRCm39) |
I4099F |
probably damaging |
Het |
| Dnah1 |
T |
A |
14: 31,022,748 (GRCm39) |
I1130F |
possibly damaging |
Het |
| Dnah12 |
A |
G |
14: 26,578,592 (GRCm39) |
K3117R |
probably benign |
Het |
| Dpf3 |
A |
T |
12: 83,319,159 (GRCm39) |
S275R |
probably benign |
Het |
| Dst |
A |
G |
1: 34,257,578 (GRCm39) |
N2450S |
probably benign |
Het |
| Dync1h1 |
C |
T |
12: 110,632,109 (GRCm39) |
R4460W |
probably damaging |
Het |
| Ecm1 |
A |
C |
3: 95,642,632 (GRCm39) |
C414G |
possibly damaging |
Het |
| Eef2 |
G |
A |
10: 81,015,384 (GRCm39) |
D302N |
probably benign |
Het |
| Egf |
T |
C |
3: 129,479,912 (GRCm39) |
D1038G |
possibly damaging |
Het |
| Epm2aip1 |
T |
C |
9: 111,101,467 (GRCm39) |
S147P |
probably damaging |
Het |
| Esam |
C |
A |
9: 37,448,863 (GRCm39) |
P324T |
possibly damaging |
Het |
| Fbxo36 |
A |
G |
1: 84,874,301 (GRCm39) |
D99G |
probably damaging |
Het |
| Fhip2a |
A |
G |
19: 57,357,017 (GRCm39) |
Y36C |
probably damaging |
Het |
| Fndc3b |
T |
C |
3: 27,515,893 (GRCm39) |
T638A |
probably benign |
Het |
| Gba2 |
T |
C |
4: 43,568,967 (GRCm39) |
T563A |
probably benign |
Het |
| Gm8180 |
T |
A |
14: 44,021,094 (GRCm39) |
N38I |
possibly damaging |
Het |
| Hs3st4 |
A |
G |
7: 123,996,249 (GRCm39) |
E305G |
probably damaging |
Het |
| Ireb2 |
T |
A |
9: 54,791,338 (GRCm39) |
F191I |
probably benign |
Het |
| Irx3 |
T |
G |
8: 92,526,625 (GRCm39) |
T360P |
probably benign |
Het |
| Itpr1 |
T |
A |
6: 108,380,357 (GRCm39) |
I1375N |
probably benign |
Het |
| Klrh1 |
A |
T |
6: 129,752,345 (GRCm39) |
F57I |
probably benign |
Het |
| Lama4 |
A |
T |
10: 38,963,369 (GRCm39) |
I1314F |
possibly damaging |
Het |
| Lamb2 |
C |
A |
9: 108,363,347 (GRCm39) |
A842D |
probably benign |
Het |
| Ldlrap1 |
A |
G |
4: 134,486,307 (GRCm39) |
Y51H |
possibly damaging |
Het |
| Leo1 |
A |
G |
9: 75,355,623 (GRCm39) |
D321G |
probably damaging |
Het |
| Lrrc14b |
A |
G |
13: 74,511,226 (GRCm39) |
S285P |
probably damaging |
Het |
| Macf1 |
A |
G |
4: 123,326,860 (GRCm39) |
V4881A |
probably benign |
Het |
| Mfsd2b |
A |
T |
12: 4,916,481 (GRCm39) |
F333I |
probably damaging |
Het |
| Micall1 |
T |
C |
15: 79,006,760 (GRCm39) |
S196P |
unknown |
Het |
| Mrps21 |
T |
C |
3: 95,770,110 (GRCm39) |
N73S |
probably benign |
Het |
| Msantd5f5 |
G |
A |
4: 73,542,736 (GRCm39) |
G79S |
probably damaging |
Het |
| Msln |
C |
T |
17: 25,969,708 (GRCm39) |
V341M |
possibly damaging |
Het |
| Mybpc3 |
A |
T |
2: 90,962,001 (GRCm39) |
M840L |
probably damaging |
Het |
| Myo7a |
A |
C |
7: 97,714,000 (GRCm39) |
F1613V |
probably damaging |
Het |
| Naprt |
C |
T |
15: 75,763,607 (GRCm39) |
|
probably null |
Het |
| Nbr1 |
T |
C |
11: 101,462,765 (GRCm39) |
V572A |
probably damaging |
Het |
| Nfkbie |
A |
T |
17: 45,870,233 (GRCm39) |
T193S |
probably damaging |
Het |
| Nlrp14 |
T |
G |
7: 106,789,251 (GRCm39) |
N672K |
probably benign |
Het |
| Or11l3 |
A |
T |
11: 58,516,260 (GRCm39) |
I204N |
probably damaging |
Het |
| Or4b1d |
A |
G |
2: 89,968,668 (GRCm39) |
Y272H |
probably damaging |
Het |
| Or52ab2 |
A |
G |
7: 102,969,656 (GRCm39) |
T13A |
|
Het |
| Or5b101 |
T |
C |
19: 13,005,439 (GRCm39) |
T85A |
probably benign |
Het |
| Or6k14 |
A |
T |
1: 173,927,299 (GRCm39) |
I92F |
probably damaging |
Het |
| Or8b49 |
A |
T |
9: 38,506,200 (GRCm39) |
I228L |
probably benign |
Het |
| Oscar |
T |
C |
7: 3,614,149 (GRCm39) |
T197A |
possibly damaging |
Het |
| P3h3 |
C |
A |
6: 124,827,594 (GRCm39) |
A481S |
possibly damaging |
Het |
| Pcdh8 |
T |
C |
14: 80,008,691 (GRCm39) |
|
probably null |
Het |
| Pcsk9 |
A |
T |
4: 106,316,094 (GRCm39) |
H116Q |
probably benign |
Het |
| Ptcd1 |
A |
G |
5: 145,091,540 (GRCm39) |
F520L |
possibly damaging |
Het |
| Rapgef2 |
T |
C |
3: 78,976,580 (GRCm39) |
T1261A |
probably benign |
Het |
| Ribc2 |
T |
A |
15: 85,019,446 (GRCm39) |
M76K |
probably benign |
Het |
| Sin3b |
A |
G |
8: 73,479,853 (GRCm39) |
E853G |
probably damaging |
Het |
| Slit2 |
A |
G |
5: 48,414,180 (GRCm39) |
D940G |
probably damaging |
Het |
| Smarcb1 |
T |
A |
10: 75,733,373 (GRCm39) |
N342Y |
probably damaging |
Het |
| Smurf2 |
A |
T |
11: 106,726,921 (GRCm39) |
I469N |
probably damaging |
Het |
| Spata31h1 |
T |
C |
10: 82,119,421 (GRCm39) |
I4530V |
probably benign |
Het |
| Spta1 |
T |
C |
1: 174,074,065 (GRCm39) |
Y2335H |
probably damaging |
Het |
| Suz12 |
C |
T |
11: 79,915,801 (GRCm39) |
R425C |
probably benign |
Het |
| Synpo |
G |
A |
18: 60,762,895 (GRCm39) |
A4V |
probably benign |
Het |
| Tet1 |
A |
C |
10: 62,649,129 (GRCm39) |
S157A |
possibly damaging |
Het |
| Themis |
A |
G |
10: 28,637,415 (GRCm39) |
E173G |
possibly damaging |
Het |
| Timmdc1 |
A |
T |
16: 38,325,780 (GRCm39) |
L197* |
probably null |
Het |
| Tmem63c |
T |
C |
12: 87,115,932 (GRCm39) |
F191S |
possibly damaging |
Het |
| Tnn |
G |
A |
1: 159,937,917 (GRCm39) |
T1200I |
probably benign |
Het |
| Traf6 |
A |
G |
2: 101,527,537 (GRCm39) |
H429R |
probably benign |
Het |
| Trem3 |
T |
C |
17: 48,556,873 (GRCm39) |
S115P |
probably benign |
Het |
| Trip11 |
A |
T |
12: 101,851,639 (GRCm39) |
N808K |
probably benign |
Het |
| Trub2 |
A |
T |
2: 29,673,385 (GRCm39) |
V106E |
probably damaging |
Het |
| Ugcg |
A |
G |
4: 59,217,156 (GRCm39) |
I227V |
probably benign |
Het |
| Vat1l |
G |
A |
8: 114,963,539 (GRCm39) |
|
probably null |
Het |
| Vmn1r184 |
T |
C |
7: 25,966,824 (GRCm39) |
M190T |
possibly damaging |
Het |
| Vmn2r3 |
T |
C |
3: 64,182,953 (GRCm39) |
T249A |
probably benign |
Het |
| Zfp729b |
A |
C |
13: 67,742,002 (GRCm39) |
S88A |
probably benign |
Het |
| Zfp995 |
T |
C |
17: 22,099,181 (GRCm39) |
Y351C |
probably 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 |
|
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 |
|
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 |
|
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'- TGACATTGTCCCTGCTCAGC -3'
(R):5'- TCTGTGTGCCTGTCAGACAC -3'
Sequencing Primer
(F):5'- TGCTCAGCTCCAGGGGAAAC -3'
(R):5'- TGTCACCCCTGCTGGAATGTG -3'
|
| Posted On |
2019-10-17 |
Incidental Mutation