Variant #0000689720 (NC_000006.11:g.33153545_33153546del, NM_080680.2:c.813_814del (COL11A2))

Chromosome 6
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.33153545_33153546del
DNA change (hg38) -
Published as COL11A2(NM_080680.2):c.813_814delCT (p.Y272Lfs*2)
ISCN -
DB-ID COL11A2_000188
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL11A2 NM_080680.2 +/. - c.813_814del r.(?) p.(Tyr272LeufsTer2)


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