Product Details

SNP ID

rs142667711

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:79970825 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTGTCGTAGAAGTTTCTTGATGA[C/G]AATACCTTCAAATGCAAATATGGTT

Phenotype

MIM: 601056

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

BCL2A1 PubMed Links

Gene Details

Gene

BCL2A1

Gene Name

BCL2 related protein A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001114735.1	477	Missense Mutation	CTC,GTC	L99V	NP_001108207.1
NM_004049.3	477	Missense Mutation	CTC,GTC	L99V	NP_004040.1

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