Variant #0000016447 (NC_000004.11:g.15529259del, NM_001080522.2:c.1339del (CC2D2A))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.15529259del
DNA change (hg38) g.15527636del
Published as 1339delG
ISCN -
DB-ID CC2D2A_000005 See all 2 reported entries
Variant remarks 1 MKS6 family with undetermined ethnicity (het)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
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 2019-02-23 21:36:08 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D2A NM_001080522.2 +/+ 13 c.1339del r.(1339del) p.(Ala447Argfs*11)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.