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SNP ID

rs116711571

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:19535922 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGTCTTGGTTCAACACTCCCTCA[A/C]AGAGCTGCTGTGAGAAGGGGCTTTC

Phenotype

MIM: 609832

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC47A1 PubMed Links

Gene Details

Gene

SLC47A1

Gene Name

solute carrier family 47 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018242.2		Intron			NP_060712.2

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