Product Details

SNP ID

rs201959823

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:156312066 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAGAGAATCTCTTTGCTAGCCCCC[C/T]GGAGGAGAATGGTGCAGGCCTTGGG

Phenotype

MIM: 600114

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CCT3 PubMed Links

Gene Details

Gene

CCT3

Gene Name

chaperonin containing TCP1 subunit 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001008800.2	1247	Missense Mutation			NP_001008800.1
NM_005998.4	1247	Missense Mutation			NP_005989.3

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