Variant #0000886474 (NC_000005.9:g.10254964A>T, NC_000005.9(NM_012073.3):c.331+14A>T (CCT5))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10254964A>T
DNA change (hg38) -
Published as CCT5(NM_001306154.2):c.166+647A>T, CCT5(NM_012073.3):c.331+14A>T
ISCN -
DB-ID CCT5_000033 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) 0.00192 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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.331+14A>T r.(=) p.(=)
FAM173B NM_199133.3 -?/. - c.-4979T>A r.(?) p.(=)


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