Variant #0000016463 (NC_000004.11:g.15599090T>A, NC_000004.11(NM_001080522.2):c.4496+2T>A (CC2D2A))

Chromosome 4
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.15599090T>A
DNA change (hg38) g.15597467T>A
Published as -
ISCN -
DB-ID CC2D2A_000021 See all 4 reported entries
Variant remarks 1 French MKS6 family (com-het); potential missplicing
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 2020-06-16 12:41:11 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D2A NM_001080522.2 +?/+? 38i c.4496+2T>A r.spl p.?


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