Product Details

SNP ID

rs61966074

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:103049298 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGCATGATTCCTTACATCCTAAGA[A/G]TATTGCGGCAAAGGCGAGCTGGAAA

Phenotype

MIM: 601295

Polymorphism

A/G, Transition 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	1507	Missense Mutation	CTC,TTC	L304F	NP_000443.1

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