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SNP ID

hCV25608814

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:103046421 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCACCATTCTTAGTTCTATGGCTA[A/C]TCATGGCGAGAGGGATGACTGCACT

Phenotype

MIM: 601295

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC10A2 PubMed Links

Gene Details

Gene

SLC10A2

Gene Name

solute carrier family 10 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000452.2		Intron			NP_000443.1

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