Product Details

SNP ID

rs199939747

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:34130599 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTGATGGGACTCTGGAGCTTTGGG[A/G]GGCTCCGGGTGGAGACTGGACACCC

Phenotype

Polymorphism

A/G, Transition 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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