Product Details

SNP ID

rs146416795

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:25845390 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCACTATCCTTTACCTTCATAAAC[A/G]AGTGAGTTTTCTCTCTTTAGCCCAT

Phenotype

MIM: 611034

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC17A3 PubMed Links

Gene Details

Gene

SLC17A3

Gene Name

solute carrier family 17 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098486.1	1365	Missense Mutation	CGT,TGT	R497C	NP_001091956.1
NM_006632.3	1365	Missense Mutation	CGT,TGT	R419C	NP_006623.2

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