Product Details

SNP ID

rs8177959

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:81082082 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCACCTTCCTCTGTCTTTCCTCTTC[C/T]TTCTTCAGACCTCGCATGATAGAAA

Phenotype

MIM: 238330

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C16orf46 PubMed Links

Additional Information

For this assay, SNP(s) [rs116820313] 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

C16orf46

Gene Name

chromosome 16 open reading frame 46

There are no transcripts associated with this gene.

Gene

GCSH

Gene Name

glycine cleavage system protein H

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004483.4	1403	UTR 3			NP_004474.2
XM_017023136.1	1403	Intron			XP_016878625.1
XM_017023137.1	1403	Intron			XP_016878626.1

View Full Product Details