Product Details

SNP ID

rs9896507

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:28489843 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAACCACTGTCTAGTTTTTAGAAAC[A/C]GCACTAAAGTATCTATCTCCCAGTC

Phenotype

MIM: 604148

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC13A2 PubMed Links

Gene Details

Gene

SLC13A2

Gene Name

solute carrier family 13 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145975.1		Intron			NP_001139447.1
NM_003984.3		Intron			NP_003975.1
XM_006722165.2		Intron			XP_006722228.1
XM_011525450.2		Intron			XP_011523752.1
XM_011525451.1		Intron			XP_011523753.1
XM_011525452.1		Intron			XP_011523754.1
XM_011525453.2		Intron			XP_011523755.1
XM_011525454.2		Intron			XP_011523756.1

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