Variant #0001027069 (NC_000017.10:g.78022555G>C, NM_017950.3:c.850G>C (CCDC40))

Chromosome 17
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.78022555G>C
DNA change (hg38) -
Published as CCDC40(NM_001243342.1):c.850G>C (p.(Asp284His)), CCDC40(NM_017950.3):c.850G>C (p.D284H)
ISCN -
DB-ID CCDC40_000110 See all 3 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) 0.00284 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC40 NM_017950.3 ?/. - c.850G>C r.(?) p.(Asp284His)


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