Variant #0000849803 (NC_000002.11:g.238289917C>T, NM_004369.3:c.1538G>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.238289917C>T
DNA change (hg38) -
Published as COL6A3(NM_004369.3):c.1538G>A (p.R513Q, p.(Arg513Gln)), COL6A3(NM_004369.4):c.1538G>A (p.R513Q)
ISCN -
DB-ID COL6A3_000483 See all 8 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) 0.00038 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL6A3 NM_004369.3 ?/. - c.1538G>A r.(?) p.(Arg513Gln)


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