Product Details

SNP ID
rs35304946
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:4087263 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCCAGAAATGGTCCATGTCCAGAC[A/G]CAAGACTGGAGTTTCTGCCACAAAT
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
C6orf201 PubMed Links
Additional Information
For this assay, SNP(s) [rs79662395] 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
C6orf201
Gene Name
chromosome 6 open reading frame 201
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001085401.2 79 Intron NP_001078870.1
XM_005249112.3 79 Intron XP_005249169.1
XM_011514613.2 79 Intron XP_011512915.1
XM_017010861.1 79 Intron XP_016866350.1
Gene
FAM217A
Gene Name
family with sequence similarity 217 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173563.2 79 Intron NP_775834.2
XM_005248951.3 79 Intron XP_005249008.1
XM_006715025.2 79 Intron XP_006715088.1
XM_006715026.3 79 Intron XP_006715089.1
XM_011514413.2 79 Intron XP_011512715.1
XM_011514414.2 79 Intron XP_011512716.1
XM_011514415.1 79 UTR 5 XP_011512717.1
XM_011514416.2 79 Intron XP_011512718.1
XM_011514417.1 79 Intron XP_011512719.1
XM_017010480.1 79 Intron XP_016865969.1
XM_017010481.1 79 Intron XP_016865970.1
XM_017010482.1 79 UTR 5 XP_016865971.1

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