Product Details

SNP ID

rs13418816

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:119287781 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTGAAGGAAGAGGTTAGATTTGGA[C/T]GCAACTGTGTGTGTTTAAAATAAAA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C2orf76 PubMed Links

Additional Information

For this assay, SNP(s) [rs76695498] are located under a probe 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

C2orf76

Gene Name

chromosome 2 open reading frame 76

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017927.3		Intron			NP_001017927.2
NM_001322329.1		Intron			NP_001309258.1
NM_001322330.1		Intron			NP_001309259.1
NM_001322331.1		Intron			NP_001309260.1
NM_001322332.1		Intron			NP_001309261.1
XM_017003354.1		Intron			XP_016858843.1

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