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SNP ID

rs200047366

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:34131299 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGACTCTCCAGTCTCCGGAGGCTCC[C/G]GGCGGAGACTGGACACCGGAGTCTT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM47A PubMed Links

Gene Details

Gene

FAM47A

Gene Name

family with sequence similarity 47 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_203408.3		Intron			NP_981953.2

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