Variant #0000559212 (NC_000016.9:g.775852A>T, NM_001031737.2:c.209T>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.775852A>T
DNA change (hg38) g.725852A>T
Published as CCDC78(NM_001031737.3):c.209T>A (p.I70N)
ISCN -
DB-ID CCDC78_000022
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.209T>A r.(?) p.(Ile70Asn)
NARFL NM_022493.1 ?/. - c.*4565T>A r.(=) p.(=)
FAM173A NM_023933.2 ?/. - c.*3295A>T r.(=) p.(=)
HAGHL NM_032304.2 ?/. - c.-1658A>T r.(?) p.(=)


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