Product Details

SNP ID

rs1627801

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:12052340 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAATTGATTAGTAAAGCTTATTCCT[C/G]TTGTCTAACTGAAACTGTGTAGCCT

Phenotype

MIM: 606126

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

BCL2L14 PubMed Links

Additional Information

For this assay, SNP(s) [rs117099781] are located under a probe and SNP(s) [rs117080167] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

BCL2L14

Gene Name

BCL2 like 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030766.1		Intron			NP_110393.1
NM_138722.1		Intron			NP_620048.1
NM_138723.1		Intron			NP_620049.1
XM_006719151.3		Intron			XP_006719214.1
XM_011520848.1		Intron			XP_011519150.1
XM_011520849.1		Intron			XP_011519151.1
XM_017019963.1		Intron			XP_016875452.1

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