Product Details

SNP ID

rs148125885

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:112886605 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGCCAAGGACAGCTGCAGTATGA[C/T]GAACACCTTTCCTGTGGAAGGGACA

Phenotype

MIM: 608956

Polymorphism

C/T, 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	1457	Missense Mutation	ATC,GTC	I409V	NP_149040.3

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