Product Details

SNP ID

rs2661874

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:33265536 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCACATCAGGACTCAGCTTGATATC[A/C]TAGGTCAACATATCTGTGCCTTCGT

Phenotype

MIM: 601497 MIM: 610900

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

BAG1 PubMed Links

Additional Information

For this assay, SNP(s) [rs111809650] 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

BAG1

Gene Name

BCL2 associated athanogene 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001172415.1		Intron			NP_001165886.1
NM_004323.5		Intron			NP_004314.5

Gene

CHMP5

Gene Name

charged multivesicular body protein 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001195536.1		Intron			NP_001182465.1
NM_016410.5		Intron			NP_057494.3

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