Product Details

SNP ID

rs201645076

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:53237453 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACATTTGTGTGGTTTCTCTCCAGGA[G/T]GTATATTCTGATGCCTAGTGAGATG

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

ZNF677 PubMed Links

Additional Information

For this assay, SNP(s) [rs8113436] 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

ZNF677

Gene Name

zinc finger protein 677

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317998.1	1686	Missense Mutation			NP_001304927.1
NM_182609.3	1686	Missense Mutation			NP_872415.1
XM_005258862.4	1686	Missense Mutation			XP_005258919.1
XM_011526912.2	1686	Missense Mutation			XP_011525214.1

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