Product Details

SNP ID
rs149590779
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:34932416 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCAAAAGCTTGGACTCCAAGACGA[G/T]CTCTTCCTTTTATACTGTTCTTATA
Phenotype
MIM: 610730
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CCT6B PubMed Links

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 1279 Missense Mutation GAT,GCT D396A NP_001180458.1
NM_001193530.1 1279 Missense Mutation GAT,GCT D388A NP_001180459.1
NM_006584.3 1279 Missense Mutation GAT,GCT D433A NP_006575.2
XM_011524203.2 1279 Missense Mutation GAT,GCT D291A XP_011522505.1
XM_017024023.1 1279 Missense Mutation GAT,GCT D367A XP_016879512.1
XM_017024024.1 1279 Missense Mutation GAT,GCT D254A XP_016879513.1

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