Variant #0000047291 (NC_000012.11:g.48398104T>C, COL2A1(NM_001844.4):c.1A>G)

Individual ID 00024502
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.48398104T>C
DNA change (hg38) g.48004321T>C
Published as -
ISCN -
DB-ID COL2A1_000231 See all 2 reported entries
Variant remarks -
Reference PubMed: Richards 2010
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL2A1 NM_001844.4 +/. 1 c.1A>G r.(?) p.M1?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000024494 DNA SEQ - - COL2A1 1 Isabelle Touitou