Variant #0000692148 (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) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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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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