Product Details

SNP ID

rs200308750

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:25849426 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGTACAATGACAGGTGCTATGCTC[A/G]AAAATCCTCTTGATGCTCCCATGAG

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	1186	Missense Mutation			NP_001091956.1
NM_006632.3	1186	Missense Mutation			NP_006623.2

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