Variant #0000016457 (NC_000004.11:g.(15569410_15570915)_(15581795_15587779)del, NC_000004.11(NM_001080522.2):c.(3398+1_3399-1)_(3975+1_3976-1)del (CC2D2A))

Chromosome 4
Allele Both (homozygous)
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.(15569410_15570915)_(15581795_15587779)del
DNA change (hg38) -
Published as deletion ex28-31
ISCN -
DB-ID CC2D2A_000015 See all 5 reported entries
Variant remarks 1 Algerian MKS6 family (hom)
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 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D2A NM_001080522.2 +/+ 27i_31i c.(3398+1_3399-1)_(3975+1_3976-1)del r.(del) p.?


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.