Product Details

SNP ID

rs9935025

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.16:68273544 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CCTTTGATAGATTCTGGGTCCTTCA[C/T]AGGTAGGTTAATGTGGAATCCAACA

Phenotype

MIM: 605641

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC7A6 PubMed Links

Gene Details

Gene

SLC7A6

Gene Name

solute carrier family 7 member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001076785.2		Intron			NP_001070253.1
NM_003983.5		Intron			NP_003974.3
XM_011523433.1		Intron			XP_011521735.1
XM_011523434.1		Intron			XP_011521736.1
XM_011523438.1		Intron			XP_011521740.1
XM_011523439.1		Intron			XP_011521741.1
XM_017023851.1		Intron			XP_016879340.1

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