Product Details

SNP ID

rs201797267

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:34639266 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTTACCTGCTGCAAAAAGCATGAC[C/T]GCAACAGGTCTATAGAAACGCCTTC

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	607	Silent Mutation	GCA,GCG	A116A	NP_113630.1

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