Product Details

SNP ID

rs187660587

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:103563113 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGCGGCGCCGAGCGCAGGGATACG[A/G]CGCCCAGCGGGGTAAGCAGGGGCCT

Phenotype

MIM: 616003 MIM: 603885

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

APOPT1 PubMed Links

Additional Information

For this assay, SNP(s) [rs2274267] are located under a probe 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

APOPT1

Gene Name

apoptogenic 1, mitochondrial

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302652.1	157	Missense Mutation	ACG,GCG	T51A	NP_001289581.1
NM_001302653.1	157	Missense Mutation	ACG,GCG	T51A	NP_001289582.1
NM_001302654.1	157	Missense Mutation	ACG,GCG	T51A	NP_001289583.1
NM_032374.4	157	Missense Mutation	ACG,GCG	T51A	NP_115750.2

Gene

BAG5

Gene Name

BCL2 associated athanogene 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001015048.2	157	Intron			NP_001015048.1
NM_001015049.2	157	Intron			NP_001015049.1
NM_004873.3	157	Intron			NP_004864.1

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