Product Details

SNP ID

rs181316271

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:34961630 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGAGTGATAAATCAGGAAGAATTG[A/C]GGCGGTTAATGAAGGAGAAGCAGCG

Phenotype

MIM: 610730

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

CCT6B PubMed Links

Additional Information

For this assay, SNP(s) [rs77056680] 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

CCT6B

Gene Name

chaperonin containing TCP1 subunit 6B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001193529.2	101	Intron			NP_001180458.1
NM_001193530.1	101	Intron			NP_001180459.1
NM_006584.3	101	Intron			NP_006575.2
XM_011524203.2	101	Intron			XP_011522505.1
XM_017024023.1	101	Intron			XP_016879512.1
XM_017024024.1	101	Intron			XP_016879513.1

Gene

ZNF830

Gene Name

zinc finger protein 830

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052857.3	101	Silent Mutation	AGG,CGG	R22R	NP_443089.3

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