Product Details

SNP ID

rs180778462

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:14644415 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGAGATGAACCTCTCAAAAGCAC[C/T]GGCCCTCAGATTTCTGTTAGTGAAT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

BFAR PubMed Links

Gene Details

Gene

BFAR

Gene Name

bifunctional apoptosis regulator

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016561.2	330	Silent Mutation	ACC,ACT	T23T	NP_057645.1
XM_005255350.2	330	UTR 5			XP_005255407.1
XM_011522520.1	330	Silent Mutation	ACC,ACT	T23T	XP_011520822.1

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