Variant #0000567904 (NC_000019.9:g.48800387del, NM_144577.3:c.1862del (CCDC114))

Chromosome 19
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.48800387del
DNA change (hg38) g.48297130del
Published as CCDC114(NM_001364171.2):c.1973del (p.(Gly658Alafs*126)), ODAD1(NM_144577.4):c.1862delG (p.G621Afs*126)
ISCN -
DB-ID CCDC114_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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC114 NM_144577.3 ?/. - c.1862del r.(?) p.(Gly621AlafsTer126)


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