Product Details

SNP ID

rs11926927

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:38268005 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGAATTAGATGGATGTTTTCAAGG[A/G]TTTGGGACCTCTGTTCTTTGGTGTT

Phenotype

MIM: 604047

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC22A13 PubMed Links

Gene Details

Gene

SLC22A13

Gene Name

solute carrier family 22 member 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004256.3		Intron			NP_004247.2
XM_017007519.1		Intron			XP_016863008.1

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