Variant #0000193763 (NC_000012.11:g.48393773_48393775delinsCC, COL2A1(NM_001844.4):c.219_221delinsGG)

Individual ID 00117352
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48393773_48393775delinsCC
DNA change (hg38) g.47999990_47999992delinsCC
Published as -
ISCN -
DB-ID COL2A1_000477 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Mouna Barat-Houari
Database submission license No license selected
Created by Mouna Barat-Houari
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL2A1 NM_001844.4 +/. 2 c.219_221delinsGG r.(?) p.(Asp74Alafs*43)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000117818 DNA SEQ blood - COL2A1 1 Mouna Barat-Houari