Product Details

SNP ID

rs6597087

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:4706428 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCTGTAACTTTAAGAGTTTGGGTG[G/T]TTTTTTTTTCTTTTCATTTGTTTGT

Phenotype

MIM: 603778

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CDYL PubMed Links

Additional Information

For this assay, SNP(s) [rs114726049] 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

CDYL

Gene Name

chromodomain protein, Y-like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143970.1		Intron			NP_001137442.1
NM_001143971.1		Intron			NP_001137443.1
NM_004824.3		Intron			NP_004815.3
XM_011514997.2		Intron			XP_011513299.1

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