Variant #0000329914 (NC_000004.11:g.15560833del, NM_001080522.2:c.2875del (CC2D2A))

Chromosome 4
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.15560833del
DNA change (hg38) g.15559210del
Published as CC2D2A(NM_001080522.2):c.2874delG (p.(Glu959AsnfsTer3)), CC2D2A(NM_001080522.2):c.2875delG (p.E959Nfs*3)
ISCN -
DB-ID CC2D2A_000029 See all 5 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D2A NM_001080522.2 ?/. - c.2875del r.(?) p.(Glu959AsnfsTer3)


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