Product Details

SNP ID

rs151021291

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:54334827 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTATGTTTTTCAGACAGCATAAA[A/C]TAGAGGATGCTGCTATAACATATGT

Phenotype

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

C2orf73 PubMed Links

Additional Information

For this assay, SNP(s) [rs141374956] 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

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	149	Missense Mutation	ATA,CTA	I13L	NP_001093866.1
XM_005264133.1	149	Intron			XP_005264190.1
XM_005264134.3	149	Intron			XP_005264191.1
XM_011532510.2	149	Missense Mutation	ATA,CTA	I13L	XP_011530812.1
XM_011532513.2	149	Intron			XP_011530815.1
XM_017003323.1	149	Missense Mutation	ATA,CTA	I13L	XP_016858812.1
XM_017003324.1	149	Missense Mutation	ATA,CTA	I13L	XP_016858813.1

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