Product Details

SNP ID

rs199561868

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:54334877 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAAGTGAAAATGAAGAAATTAAACA[C/T]GAAGAAAAACCTGGAAAAAGCATAC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C2orf73 PubMed Links

Additional Information

For this assay, SNP(s) [rs55714450] 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

C2orf73

Gene Name

chromosome 2 open reading frame 73

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001100396.1	199	Silent Mutation	CAC,CAT	H29H	NP_001093866.1
XM_005264133.1	199	Intron			XP_005264190.1
XM_005264134.3	199	Intron			XP_005264191.1
XM_011532510.2	199	Silent Mutation	CAC,CAT	H29H	XP_011530812.1
XM_011532513.2	199	Intron			XP_011530815.1
XM_017003323.1	199	Intron			XP_016858812.1
XM_017003324.1	199	Silent Mutation	CAC,CAT	H29H	XP_016858813.1

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