Product Details

SNP ID

rs200126594

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:30198487 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCATTCAAGCGGATGTCCCCACAA[A/G]GAATTTCTGTTGGTGTTTCTGGGGT

Phenotype

MIM: 182138

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC6A4 PubMed Links

Gene Details

Gene

SLC6A4

Gene Name

solute carrier family 6 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001045.5	2438	Missense Mutation	CCT,CTT	P621L	NP_001036.1

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