Variant #0000016446 (NC_000004.11:g.15516446del, NM_001080522.2:c.834del (CC2D2A))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.15516446del
DNA change (hg38) g.15514823del
Published as Leu279CysfsX40
ISCN -
DB-ID CC2D2A_000004
Variant remarks 1 American MKS6 family (het)
Reference PubMed: Mougou-Zerelli et al. 2009
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-11-15 14:05:58 +01:00 (CET)
Date last edited 2020-06-16 12:40:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D2A NM_001080522.2 +/+ 12 c.834del r.(?) p.(Leu279Cysfs*40)


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