Product Details

SNP ID

rs78096730

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:2815133 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCCTACCCCTTCCCCTACTCTCA[C/T]CCTTATAATCCTTTTCAGCACTAGG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C20orf141 PubMed Links

Additional Information

For this assay, SNP(s) [rs116718424] 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

C20orf141

Gene Name

chromosome 20 open reading frame 141

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256538.1	123	Intron			NP_001243467.1
NM_080739.2	123	UTR 5			NP_542777.1

Gene

TMEM239

Gene Name

transmembrane protein 239

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001167670.2	123	Intron			NP_001161142.1
NM_001318207.1	123	Intron			NP_001305136.1
XM_011529128.2	123	Intron			XP_011527430.1
XM_011529129.2	123	Intron			XP_011527431.1

View Full Product Details