Product Details

SNP ID

rs149881406

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:47432396 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAGTGCATCACGTAGTCAAAGCA[C/T]GACGGCAGCCGCTCCTCCCGGGACC

Phenotype

MIM: 601901

Polymorphism

C/T, 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	2229	Silent Mutation			NP_055878.1
XM_005259172.1	2229	Silent Mutation			XP_005259229.1
XM_017027159.1	2229	Silent Mutation			XP_016882648.1

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