Variant #0000567913 (NC_000019.9:g.48807210C>T, NM_144577.3:c.742G>A (CCDC114))

Chromosome 19
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.48807210C>T
DNA change (hg38) g.48303953C>T
Published as CCDC114(NM_001364171.2):c.853G>A (p.(Ala285Thr)), CCDC114(NM_144577.4):c.742G>A (p.A248T), ODAD1(NM_144577.4):c.742G>A (p.A248T)
ISCN -
DB-ID CCDC114_000001 See all 4 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) 0.00024 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.742G>A r.(?) p.(Ala248Thr)


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