Variant #0000270499 (NC_000021.8:g.47552209G>A, NM_001849.3:c.2803G>A (COL6A2))

Chromosome 21
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47552209G>A
DNA change (hg38) g.46132295G>A
Published as COL6A2(NM_001849.3):c.2803G>A (p.G935R), COL6A2(NM_001849.4):c.2803G>A (p.G935R)
ISCN -
DB-ID COL6A2_000118 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) 0.07956 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL6A2 NM_001849.3 -/. - c.2803G>A r.(?) p.(Gly935Arg)
FTCD NM_006657.2 -/. - c.*4202C>T r.(=) p.(=)


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