Product Details

SNP ID

rs4908803

Assay Type

Validated

NCBI dbSNP Submissions

72

Location

Chr.1:9000111 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTGGTGAAAAATGTGAGACCCAAAG[A/G]AAGATATTGAGGTGGGTTTAAACTA

Phenotype

MIM: 610371

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC2A7 PubMed Links

Gene Details

Gene

SLC2A7

Gene Name

solute carrier family 2 member 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207420.2		Intron			NP_997303.2
XM_011540824.2		Intron			XP_011539126.1
XM_011540825.2		Intron			XP_011539127.1

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