Variant #0001055299 (NC_000016.9:g.775136C>A, NM_001031737.2:c.502G>T (CCDC78))

Chromosome 16
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.775136C>A
DNA change (hg38) -
Published as CCDC78(NM_001378030.1):c.502G>T (p.(Glu168*))
ISCN -
DB-ID CCDC78_000053
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) 2.0E-5 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 2025-11-01 13:22:20 +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     
CCDC78 NM_001031737.2 ?/. - c.502G>T r.(?) p.(Glu168*)
NARFL NM_022493.1 ?/. - c.*5281G>T r.(=) p.(=)
FAM173A NM_023933.2 ?/. - c.*2579C>A r.(=) p.(=)
HAGHL NM_032304.2 ?/. - c.-2374C>A r.(?) p.(=)


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