Product Details

SNP ID

rs200449770

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:27081258 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGTCTTTTCGTTGGTGCTGACCG[A/G]TGGGGACTTTTGGTGGCATTCACAG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C12orf71 PubMed Links

Additional Information

For this assay, SNP(s) [rs708165] 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

C12orf71

Gene Name

chromosome 12 open reading frame 71

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080406.1	1307	Silent Mutation			NP_001073875.1
XM_011520847.2	1307	Silent Mutation			XP_011519149.1

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