Variant #0000559165 (NC_000016.9:g.771441G>A, NM_001031737.2:c.*1329C>T (CCDC78))

Chromosome 16
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.771441G>A
DNA change (hg38) g.721441G>A
Published as FAM173A(NM_001271285.1):c.162+5G>A (p.?)
ISCN -
DB-ID CCDC78_000014
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) 0.00215 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-07 12:07:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC78 NM_001031737.2 -?/. - c.*1329C>T r.(=) p.(=)
FAM173A NM_023933.2 -?/. - c.162+5G>A r.spl? p.?
METRN NM_024042.2 -?/. - c.*4054G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.