Product Details

SNP ID

rs140563330

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:22338580 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTTGGCCCCAGGAAAAGAGGGGC[G/T]AAAGAATTTTGCTGGAAAATCACTC

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	460	Missense Mutation	CGA,CTA	R16L	NP_065079.1

View Full Product Details