Variant #0000016466 (NC_000004.11:g.15513014_15513016del, NM_001080522.2:c.685_687del (CC2D2A))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.15513014_15513016del
DNA change (hg38) g.15511391_15511393del
Published as 685_7delGAA (E229del)
ISCN -
DB-ID CC2D2A_000024
Variant remarks 1 British MKS6 family (com-het)
Reference PubMed: Otto et al. 2011
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 12:40:18 +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 +?/+? 11 c.685_687del r.(?) p.(Glu229del)


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