Product Details

SNP ID

rs6699631

Assay Type

Functionally tested

NCBI dbSNP Submissions

44

Location

Chr.1:233910857 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTTTTTTCCAGAATGTGAATGGA[A/T]TGAGTTTTAAGTCATTTGTAGAATG

Phenotype

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

SLC35F3 PubMed Links

Gene Details

Gene

SLC35F3

Gene Name

solute carrier family 35 member F3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300845.1		Intron			NP_001287774.1
NM_173508.3		Intron			NP_775779.1

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