Product Details

SNP ID
hCV25954253
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:73207792 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGTTTGAAAGCTCAAACAGCTTG[G/T]CTTCTTACAGCATCGAGTTGTTTGC
Phenotype
MIM: 606973
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
COG1 PubMed Links
Additional Information
For this assay, SNP(s) [rs71710311] 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
COG1
Gene Name
component of oligomeric golgi complex 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018714.2 2286 Intron NP_061184.1
Gene
FAM104A
Gene Name
family with sequence similarity 104 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098832.1 2286 UTR 3 NP_001092302.1
NM_001289410.1 2286 UTR 3 NP_001276339.1
NM_001289411.1 2286 UTR 3 NP_001276340.1
NM_001289412.1 2286 UTR 3 NP_001276341.1
NM_032837.2 2286 UTR 3 NP_116226.2

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