Product Details

SNP ID

rs9656982

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:86214471 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAATAGTAATTGTAAATAGCAAGTC[A/G]TCTTCTCAAACCAAGCCAATCTTAT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC7A13 PubMed Links

Gene Details

Gene

SLC7A13

Gene Name

solute carrier family 7 member 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138817.2	1431	Missense Mutation	ACG,ATG	T452M	NP_620172.2
XM_011516867.1	1431	Missense Mutation	ACG,ATG	T443M	XP_011515169.1

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