Product Details

Assay Reference Genome Location: Chr.19:16204515 on build GRCh38
Cytoband: 19p13.11
Species: Homo sapiens
Variation Type: Copy Number

Additional Information

For this assay, SNP(s) [rs111700422] are located under a primer or 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.

Target Gene Details

Entrez Gene ID: 8907
Gene Symbol: AP1M1
Gene Name: adaptor related protein complex 1 mu 1 subunit
Gene Aliases: AP47, CLAPM2, CLTNM, MU-1A
Location: Chr.19:16197854-16235345 on build GRCh38
Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Protein ID
AP1M1	NM_001130524.1	NP_001123996.1
	NM_032493.3	NP_115882.1
	XM_017027420.1	XP_016882909.1
	XM_017027421.1	XP_016882910.1
	AB209808.1	BAD93045.1
	AF290613.1	AAK28024.1
	AK027528.1
	AK293188.1
	AK297824.1
	BC017469.2	AAH17469.1
	DC386056.1
	DQ059565.1	AAY54246.1

Target Copy Number Variation Details

DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv833767	Chr19:16121391 - 16347760 on Build GRCh38	Loss	FAM32A HSH2D AP1M1 RAB8A KLF2 CIB3

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