Product Details

SNP ID

rs5935996

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:15637334 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATTTTCAGGGCTCTCCCCACTTCA[A/G]ACTGCACCCTCTCCTCACATTTGAC

Phenotype

MIM: 300631

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TMEM27 PubMed Links

Gene Details

Gene

TMEM27

Gene Name

transmembrane protein 27

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020665.5		Intron			NP_065716.1
XM_017029680.1		Intron			XP_016885169.1
XM_017029681.1		Intron			XP_016885170.1

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