Product Details

SNP ID

rs12329521

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:60054704 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTTGCAGGGAGTCTGACGTTGCTCG[C/G]TAAGTCTCTTTGGTCGTTTCATACT

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

C20orf197 PubMed Links

Additional Information

For this assay, SNP(s) [rs79490303] 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

C20orf197

Gene Name

chromosome 20 open reading frame 197

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302813.1	2871	Intron			NP_001289742.1
NM_001302815.1	2871	Intron			NP_001289744.1
NM_173644.2	2871	Intron			NP_775915.1
XM_017027828.1	2871	Intron			XP_016883317.1
XM_017027829.1	2871	UTR 5			XP_016883318.1
XM_017027830.1	2871	UTR 5			XP_016883319.1
XM_017027831.1	2871	Intron			XP_016883320.1
XM_017027832.1	2871	Intron			XP_016883321.1

View Full Product Details