Variant #0000337380 (NC_000003.11:g.180337760T>A, NC_000003.11(NM_181426.1):c.1999-2A>T (CCDC39))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.180337760T>A
DNA change (hg38) g.180619972T>A
Published as -
ISCN -
DB-ID CCDC39_000032
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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-16 09:11:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTC14 NM_133462.3 +/. - c.*9430T>A r.(=) p.(=)
CCDC39 NM_181426.1 +/. - c.1999-2A>T r.spl? p.?


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