Product Details

SNP ID

rs13018263

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:102475811 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGCCAATTACTGGGCTGGTAGTTT[C/T]ATGTATAAGGGCTTGTTTACTAGGG

Phenotype

MIM: 600531

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC9A4 PubMed Links

Gene Details

Gene

SLC9A4

Gene Name

solute carrier family 9 member A4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001011552.3		Intron			NP_001011552.2
XM_011511158.1		Intron			XP_011509460.1

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