Variant #0000047247 (NC_000012.11:g.48393802G>T, COL2A1(NM_001844.4):c.192C>A)

Individual ID 00024458
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.48393802G>T
DNA change (hg38) g.48000019G>T
Published as -
ISCN -
DB-ID COL2A1_000175 See all 5 reported entries
Variant remarks -
Reference PubMed: McAlinden 2008
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Isabelle Touitou
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL2A1 NM_001844.4 +/. 2 c.192C>A r.(?) p.(Cys64*)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000024450 DNA SEQ - - COL2A1 1 Isabelle Touitou