Product Details

SNP ID

rs16956134

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:6686779 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTTCCCTCATGGTCACTAACCATC[A/G]CTTCACTACCCTGTTGTAGATATTT

Phenotype

MIM: 608305

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC13A5 PubMed Links

Gene Details

Gene

SLC13A5

Gene Name

solute carrier family 13 member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143838.2		Intron			NP_001137310.1
NM_001284509.1		Intron			NP_001271438.1
NM_001284510.1		Intron			NP_001271439.1
NM_177550.4		Intron			NP_808218.1
XM_011523795.2		Intron			XP_011522097.1

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