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SNP ID

rs150237752

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:33056517 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGTGAGGTTGGAGTTTCTAGTAC[C/T]TTCCTACTTCCACTCTCTCTGCAGC

Phenotype

MIM: 615717

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

BPIFB3 PubMed Links

Gene Details

Gene

BPIFB3

Gene Name

BPI fold containing family B member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182658.2		Intron			NP_872599.1

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