Product Details

SNP ID

rs78579480

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:10613765 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAGGTGGGTTTGATGTGATTGCTG[G/T]CTTTAAAAATGGAAGAAGTGGCCAG

Phenotype

MIM: 606106

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SLC44A2 PubMed Links

Gene Details

Gene

SLC44A2

Gene Name

solute carrier family 44 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145056.1		Intron			NP_001138528.1
NM_020428.3		Intron			NP_065161.3
XM_005259997.1		Intron			XP_005260054.1
XM_005259999.1		Intron			XP_005260056.1

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