Variant #0000346206 (NC_000001.10:g.103468815C>A, COL11A1(NM_001190709.1):c.1837G>T)

Chromosome 1
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.103468815C>A
DNA change (hg38) g.103003259C>A
Published as -
ISCN -
DB-ID COL11A1_000115
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL11A1 NM_001190709.1 +/. - c.1837G>T r.(?) p.(Gly613Cys)
COL11A1 NM_080629.2 +/. - c.1990G>T r.(?) p.(Gly664Cys)