Product Details

SNP ID

rs6976922

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:38389582 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGAAAGTGGTTACGTGATAAGAAA[A/C]AGTCAACTGTTTGTATTATATAAAA

Phenotype

MIM: 600418

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

AMPH PubMed Links

Additional Information

For this assay, SNP(s) [rs74561549] 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

AMPH

Gene Name

amphiphysin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001635.3		Intron			NP_001626.1
NM_139316.2		Intron			NP_647477.1
XM_006715689.3		Intron			XP_006715752.1
XM_006715690.3		Intron			XP_006715753.1
XM_006715691.3		Intron			XP_006715754.1
XM_011515271.2		Intron			XP_011513573.1
XM_017011995.1		Intron			XP_016867484.1
XM_017011996.1		Intron			XP_016867485.1

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