Product Details

SNP ID

rs145687206

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:22341610 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCCTAGAGGTGCCCGAGAGGAAG[G/T]CGCCGCTGTGCGACTGCACGTGCTT

Phenotype

MIM: 607563

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SLC17A6 PubMed Links

Gene Details

Gene

SLC17A6

Gene Name

solute carrier family 17 member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020346.2	582	Missense Mutation	GCG,TCG	A57S	NP_065079.1

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