Variant #0001041363 (NC_000016.9:g.772985C>T, NM_001031737.2:c.1234G>A (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.772985C>T
DNA change (hg38) -
Published as CCDC78(NM_001378030.1):c.1238G>A (p.(Arg413Gln))
ISCN -
DB-ID CCDC78_000045
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) 0.00038 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 2025-05-05 21:14:00 +02:00 (CEST)
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.1234G>A r.(?) p.(Gly412Arg)
FAM173A NM_023933.2 -?/. - c.*428C>T r.(=) p.(=)
METRN NM_024042.2 -?/. - c.*5598C>T r.(=) p.(=)
HAGHL NM_032304.2 -?/. - c.-4525C>T r.(?) p.(=)


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