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SNP ID

rs3802493

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:112887240 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCAAAGATGCTTCTGGAACTGTCT[T/C]AAGTGCCTTCTGCAGGTCTGTGCCT

Phenotype

MIM: 608956

Polymorphism

T/C, Transition substitution

Allele Nomenclature

Literature Links

SLC46A2 PubMed Links

Gene Details

Gene

SLC46A2

Gene Name

solute carrier family 46 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033051.3		Intron			NP_149040.3

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