Variant #0000272765 (NC_000003.11:g.180349295C>T, NM_181426.1:c.1960G>A (CCDC39))

Chromosome 3
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.180349295C>T
DNA change (hg38) g.180631507C>T
Published as CCDC39(NM_181426.1):c.1960G>A (p.(Gly654Arg)), CCDC39(NM_181426.2):c.1960G>A (p.G654R)
ISCN -
DB-ID CCDC39_000016 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) 5.0E-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 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC39 NM_181426.1 ?/. - c.1960G>A r.(?) p.(Gly654Arg)


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