Product Details

SNP ID

rs2236942

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:50211374 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTCCTAGACCTGGCCTTTACAGCT[C/G]TATCAGGTTTGTCTGTTGCCACAGA

Phenotype

MIM: 604437

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC38A3 PubMed Links

Gene Details

Gene

SLC38A3

Gene Name

solute carrier family 38 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006841.5		Intron			NP_006832.1
XM_006712954.2		Intron			XP_006713017.1

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