Variant #0000523623 (NC_000005.9:g.10254788C>T, NM_012073.3:c.169C>T (CCT5))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.10254788C>T
DNA change (hg38) g.10254676C>T
Published as CCT5(NM_001306156.2):c.55C>T (p.L19F)
ISCN -
DB-ID CCT5_000023
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCT5 NM_012073.3 ?/. - c.169C>T r.(?) p.(Leu57Phe)
FAM173B NM_199133.3 ?/. - c.-4803G>A r.(?) p.(=)


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