Variant #0000982092 (NC_000016.9:g.775236C>T, NC_000016.9(NM_001031737.2):c.492+1G>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.775236C>T
DNA change (hg38) -
Published as CCDC78(NM_001031737.2):c.492+1G>A, CCDC78(NM_001378030.1):c.492+1G>A
ISCN -
DB-ID CCDC78_000034 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) 0.00237 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 2024-04-19 20:27:30 +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.492+1G>A r.spl? p.?
NARFL NM_022493.1 -?/. - c.*5181G>A r.(=) p.(=)
FAM173A NM_023933.2 -?/. - c.*2679C>T r.(=) p.(=)
HAGHL NM_032304.2 -?/. - c.-2274C>T r.(?) p.(=)


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