Product Details

SNP ID

rs181950167

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:14648393 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTTTTCTATTCTCCATAGGGATG[C/T]CATTGAAAAGTTATTTCCTGATGCC

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	550	Missense Mutation	GCC,GTC	A90V	NP_057645.1
XM_005255350.2	550	Intron			XP_005255407.1
XM_011522520.1	550	Intron			XP_011520822.1

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