Variant #0000831391 (NC_000021.8:g.47552411_47552412del, NM_001849.3:c.3005_3006del (COL6A2))

Chromosome 21
Allele Paternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.47552411_47552412del
DNA change (hg38) g.46132497_46132498del
Published as c.3004_3005del
ISCN -
DB-ID COL6A2_000064 See all 3 reported entries
Variant remarks -
Reference PubMed: Fan 2018
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-12-29 09:59:04 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL6A2 NM_001849.3 +?/. 28 c.3005_3006del r.(?) p.(Tyr1002Ter)


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