Product Details

SNP ID

rs76745166

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:62525349 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACTTTTCCATGGGAAGGTGGGGAG[G/T]AGGTTTCAGTAAGAGTGAGAACTGT

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

ZCCHC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs78779979] 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

ZCCHC2

Gene Name

zinc finger CCHC-type containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017742.5	530	Intron			NP_060212.4
XM_006722493.3	530	Intron			XP_006722556.1
XM_011526044.1	530	UTR 5			XP_011524346.1
XM_017025802.1	530	Intron			XP_016881291.1

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