Variant #0000268056 (NC_000017.10:g.78013765del, NM_017950.3:c.248del (CCDC40))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78013765del
DNA change (hg38) g.80039966del
Published as CCDC40(NM_017950.4):c.248delC (p.A83Vfs*84)
ISCN -
DB-ID CCDC40_000020
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) 0.00045 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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     
CCDC40 NM_017950.3 +/. - c.248del r.(?) p.(Ala83ValfsTer84)
TBC1D16 NM_019020.2 +/. - c.-4234del r.(?) p.(=)


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