Variant #0000340149 (NC_000021.8:g.47552103G>T, NM_001849.3:c.2697G>T (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.47552103G>T
DNA change (hg38) g.46132189G>T
Published as COL6A2(NM_001849.3):c.2697G>T (p.(Thr899=)), COL6A2(NM_001849.4):c.2697G>T (p.T899=)
ISCN -
DB-ID COL6A2_000039 See all 21 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) 0.03435 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.2697G>T r.(?) p.(Thr899=)
FTCD NM_006657.2 -/. - c.*4308C>A r.(=) p.(=)


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