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SNP ID

rs209023

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:10449827 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGGGTGGAGATGCCATACACTTT[T/C]GAACAACCAGATCTTGTGAGAACTC

Phenotype

Polymorphism

T/C, Transition substitution

Allele Nomenclature

Literature Links

BAGE2 PubMed Links

Gene Details

Gene

BAGE2

Gene Name

B melanoma antigen family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182482.2		Intron			NP_872288.2

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