Product Details

SNP ID

rs4461908

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:23245695 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTTATAAAAGAGATGGCACAGAAC[G/T]GGTACAACTTTTTTCTTAAATATTT

Phenotype

MIM: 611130

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CHMP7 PubMed Links

Additional Information

For this assay, SNP(s) [rs7464232] 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

CHMP7

Gene Name

charged multivesicular body protein 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317899.1		Intron			NP_001304828.1
NM_152272.4		Intron			NP_689485.1
XM_006716415.2		Intron			XP_006716478.1
XM_017013961.1		Intron			XP_016869450.1
XM_017013962.1		Intron			XP_016869451.1
XM_017013963.1		Intron			XP_016869452.1
XM_017013964.1		Intron			XP_016869453.1
XM_017013965.1		Intron			XP_016869454.1

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