Product Details

SNP ID

rs10846000

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:7824755 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAAAAAAAAAAAAAAAGAATACAT[C/T]GTTTGCACAAAAGTAGGTTGGAAAA

Phenotype

MIM: 611039

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC2A14 PubMed Links

Gene Details

Gene

SLC2A14

Gene Name

solute carrier family 2 member 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286233.1		Intron			NP_001273162.1
NM_001286234.1		Intron			NP_001273163.1
NM_001286235.1		Intron			NP_001273164.1
NM_001286236.1		Intron			NP_001273165.1
NM_001286237.1		Intron			NP_001273166.1
NM_153449.3		Intron			NP_703150.1
XM_005253315.3		Intron			XP_005253372.1
XM_005253317.4		Intron			XP_005253374.1
XM_011520562.1		Intron			XP_011518864.1
XM_011520563.2		Intron			XP_011518865.1
XM_011520564.2		Intron			XP_011518866.1
XM_011520565.2		Intron			XP_011518867.1
XM_017018841.1		Intron			XP_016874330.1
XM_017018842.1		Intron			XP_016874331.1
XM_017018843.1		Intron			XP_016874332.1
XM_017018844.1		Intron			XP_016874333.1
XM_017018845.1		Intron			XP_016874334.1
XM_017018846.1		Intron			XP_016874335.1
XM_017018847.1		Intron			XP_016874336.1

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