Product Details

SNP ID

rs4987865

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:63124324 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAATATCCTGTTAGTTAAAACTGCA[C/T]ATTTATTGTTTAAATACCCATTAGA

Phenotype

MIM: 151430

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

BCL2 PubMed Links

Gene Details

Gene

BCL2

Gene Name

BCL2, apoptosis regulator

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000633.2	5514	UTR 3			NP_000624.2
NM_000657.2	5514	Intron			NP_000648.2
XM_011526135.2	5514	Intron			XP_011524437.1
XM_017025917.1	5514	Intron			XP_016881406.1

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