Product Details

SNP ID

rs201421765

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:86828129 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCGCCAGGACCACACCAGCAACTG[C/T]GACCACCAGAAGGAGGACCCCACCA

Phenotype

MIM: 613366

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC10A6 PubMed Links

Gene Details

Gene

SLC10A6

Gene Name

solute carrier family 10 member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_197965.2	773	Missense Mutation	ACA,GCA	T209A	NP_932069.1

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