Variant #0000992689 (NC_000002.11:g.238280758C>T, NM_004369.3:c.3902G>A (COL6A3))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.238280758C>T
DNA change (hg38) -
Published as COL6A3(NM_004369.3):c.3902G>A (p.R1301Q, p.(Arg1301Gln))
ISCN -
DB-ID COL6A3_000415 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) 0.00026 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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     
COL6A3 NM_004369.3 ?/. - c.3902G>A r.(?) p.(Arg1301Gln)


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