Product Details

SNP ID

rs698705

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:47434209 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAGAGGTGGCTGCTATTACCGCATC[A/G]CTATGTCAGTTGAGGCTTCTGCCTG

Phenotype

MIM: 601901

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC8A2 PubMed Links

Gene Details

Gene

SLC8A2

Gene Name

solute carrier family 8 member A2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015063.2		Intron			NP_055878.1
XM_005259172.1		Intron			XP_005259229.1
XM_017027159.1		Intron			XP_016882648.1

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