Product Details

SNP ID

rs6628886

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.X:34636660 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACTGTCAGTTACACAAAAAGAAATA[C/T]GCTGTAGTCAACTGTACTGGAAATG

Phenotype

MIM: 300698

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TMEM47 PubMed Links

Gene Details

Gene

TMEM47

Gene Name

transmembrane protein 47

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031442.3		Intron			NP_113630.1

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