Product Details

SNP ID

rs4838930

Assay Type

Functionally tested

NCBI dbSNP Submissions

36

Location

Chr.1:110158099 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATATTTGTCTGATTTCTATTTGTCC[C/G]TCTGCACTAGAAATAAATCCAATGG

Phenotype

MIM: 610299

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC6A17 PubMed Links

Gene Details

Gene

SLC6A17

Gene Name

solute carrier family 6 member 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010898.2		Intron			NP_001010898.1
XM_006710643.2		Intron			XP_006710706.1

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