Product Details

SNP ID

rs6962039

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.7:123114304 on Build GRCh38

Set Membership

HapMap DME Validated Inventoried

Context Sequence [VIC/FAM]

GATATATAATATTTGTACATATTTT[A/G]GGGGTGTATGTGATATTTTGCTACC

Phenotype

MIM: 606193

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC13A1 PubMed Links

Gene Details

Gene

SLC13A1

Gene Name

solute carrier family 13 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001324400.1	3528	UTR 3			NP_001311329.1
NM_022444.3	3528	UTR 3			NP_071889.2
XM_011516515.2	3528	UTR 3			XP_011514817.1
XM_011516516.2	3528	UTR 3			XP_011514818.1
XM_011516517.2	3528	UTR 3			XP_011514819.1
XM_011516518.2	3528	Intron			XP_011514820.1
XM_011516519.2	3528	Intron			XP_011514821.1
XM_017012554.1	3528	UTR 3			XP_016868043.1
XM_017012555.1	3528	Intron			XP_016868044.1

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