Product Details

SNP ID

rs4644485

Assay Type

Functionally tested

NCBI dbSNP Submissions

71

Location

Chr.1:15240307 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTCTTTCTGATACCCTCAAAAAAA[C/T]GAATCTTACCAATAACAATGTGAGC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FHAD1 PubMed Links

Gene Details

Gene

FHAD1

Gene Name

forkhead associated phosphopeptide binding domain 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052929.1		Intron			NP_443161.1
XM_011540575.2		Intron			XP_011538877.1
XM_011540576.2		Intron			XP_011538878.1
XM_011540577.2		Intron			XP_011538879.1
XM_011540580.2		Intron			XP_011538882.1
XM_011540581.2		Intron			XP_011538883.1
XM_011540582.2		Intron			XP_011538884.1
XM_011540584.2		Intron			XP_011538886.1
XM_011540588.2		Intron			XP_011538890.1
XM_011540589.2		Intron			XP_011538891.1
XM_011540590.2		Intron			XP_011538892.1
XM_011540592.2		Intron			XP_011538894.1
XM_011540593.2		Intron			XP_011538895.1
XM_011540595.2		Intron			XP_011538897.1
XM_011540596.2		Intron			XP_011538898.1
XM_011540597.2		Intron			XP_011538899.1
XM_011540598.2		Intron			XP_011538900.1
XM_017000198.1		Intron			XP_016855687.1
XM_017000199.1		Intron			XP_016855688.1
XM_017000200.1		Intron			XP_016855689.1
XM_017000201.1		Intron			XP_016855690.1
XM_017000202.1		Intron			XP_016855691.1
XM_017000203.1		Intron			XP_016855692.1
XM_017000204.1		Intron			XP_016855693.1
XM_017000205.1		Intron			XP_016855694.1
XM_017000206.1		Intron			XP_016855695.1
XM_017000207.1		Intron			XP_016855696.1
XM_017000208.1		Intron			XP_016855697.1
XM_017000209.1		Intron			XP_016855698.1
XM_017000210.1		Intron			XP_016855699.1
XM_017000211.1		Intron			XP_016855700.1
XM_017000212.1		Intron			XP_016855701.1
XM_017000213.1		Intron			XP_016855702.1
XM_017000214.1		Intron			XP_016855703.1

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