Product Details

SNP ID

rs201510794

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:70925927 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGGCTGTGCTGGATCCCATAGCC[A/G]AAGTAGATAGCAAAGCCTAGTGGGG

Phenotype

MIM: 300443

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC7A3 PubMed Links

Gene Details

Gene

SLC7A3

Gene Name

solute carrier family 7 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001048164.2	1920	Silent Mutation	TTC,TTT	F582F	NP_001041629.1
NM_032803.5	1920	Silent Mutation	TTC,TTT	F582F	NP_116192.4
XM_017029912.1	1920	Silent Mutation	TTC,TTT	F582F	XP_016885401.1

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