Product Details

SNP ID

rs2293952

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.X:48461915 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CAGACACATAGAAGCTCCCAATGTC[G/C]AATATCCAGCTCCACTCTGAGCAGG

Phenotype

MIM: 300649

Polymorphism

G/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC38A5 PubMed Links

Gene Details

Gene

SLC38A5

Gene Name

solute carrier family 38 member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033518.3		Intron			NP_277053.2
XM_005272694.3		Intron			XP_005272751.2
XM_005272695.4		Intron			XP_005272752.3
XM_005272697.2		Intron			XP_005272754.2
XM_005272698.4		Intron			XP_005272755.2
XM_006724569.3		Intron			XP_006724632.1
XM_017029960.1		Intron			XP_016885449.1
XM_017029961.1		Intron			XP_016885450.1

View Full Product Details