Variant #0000272806 (NC_000016.9:g.776367T>C, NM_001031737.2:c.1A>G (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.776367T>C
DNA change (hg38) g.726367T>C
Published as CCDC78(NM_001031737.2):c.1A>G (p.M1?)
ISCN -
DB-ID CCDC78_000012
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) 3.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-07 12:15:05 +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.1A>G r.(?) p.(Met1?)
NARFL NM_022493.1 ?/. - c.*4050A>G r.(=) p.(=)
FAM173A NM_023933.2 ?/. - c.*3810T>C r.(=) p.(=)
HAGHL NM_032304.2 ?/. - c.-1143T>C r.(?) p.(=)


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