Variant #0001013697 (NC_000002.11:g.238296777del, NM_004369.3:c.761del (COL6A3))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.238296777del
DNA change (hg38) -
Published as COL6A3(NM_004369.4):c.761del (p.(Gly254GlufsTer13)), COL6A3(NM_004369.4):c.761delG (p.G254Efs*13)
ISCN -
DB-ID COL6A3_000509 See all 5 reported entries
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 20:49:11 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL6A3 NM_004369.3 +?/. - c.761del r.(?) p.(Gly254Glufs*13)


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