Variant #0000047211 (NC_000012.11:g.48393757del, COL2A1(NM_001844.4):c.237del)

Individual ID 00024422
Chromosome 12
Allele Parent #1
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.48393757del
DNA change (hg38) g.47999974del
Published as 237delG
ISCN -
DB-ID COL2A1_000139
Variant remarks -
Reference PubMed: Yoshida 2006
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 Johan den Dunnen
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.237del r.(?) p.(Ile80Serfs*37)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000024414 DNA SEQ - - COL2A1 1 Johan den Dunnen