Product Details

SNP ID
rs7632655
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:63201912 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTTCCCCCCTTTTTTTCTACTGA[A/G]TTGGTTACTTTCACTCACAAAAAGA
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SYNPR PubMed Links
Additional Information
For this assay, SNP(s) [rs148880213] 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
SYNPR
Gene Name
synaptoporin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130003.1 Intron NP_001123475.1
NM_144642.4 Intron NP_653243.1
XM_017005731.1 Intron XP_016861220.1
XM_017005732.1 Intron XP_016861221.1

View Full Product Details