Variant #0000246320 (NC_000005.9:g.10254817A>G, NM_012073.3:c.198A>G (CCT5))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10254817A>G
DNA change (hg38) g.10254705A>G
Published as CCT5(NM_001306156.2):c.84A>G (p.G28=), CCT5(NM_012073.5):c.198A>G (p.G66=)
ISCN -
DB-ID CCT5_000006 See all 2 reported entries
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) 0.79933 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCT5 NM_012073.3 -/. - c.198A>G r.(?) p.(Gly66=)
FAM173B NM_199133.3 -/. - c.-4832T>C r.(?) p.(=)


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