Product Details

SNP ID

rs7842666

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:27772635 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GACTCGCGGCGGCCGCCTGGCCCCC[A/G]GAACTCCTCCGTGCACTTCCGGCGG

Phenotype

MIM: 609353

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CCDC25 PubMed Links

Additional Information

For this assay, SNP(s) [rs114445285] 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

CCDC25

Gene Name

coiled-coil domain containing 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304529.1	19	UTR 5			NP_001291458.1
NM_001304530.1	19	UTR 5			NP_001291459.1
NM_001304532.1	19	UTR 5			NP_001291461.1
NM_018246.2	19	UTR 5			NP_060716.2
XM_011544570.2	19	Intron			XP_011542872.1
XM_011544571.2	19	Intron			XP_011542873.1

Gene

ESCO2

Gene Name

establishment of sister chromatid cohesion N-acetyltransferase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017420.2	19	Intron			NP_001017420.1
XM_011544421.2	19	Intron			XP_011542723.1
XM_011544422.2	19	Intron			XP_011542724.1

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