Variant #0000328762 (NC_000021.8:g.47552423C>T, NM_001849.3:c.3017C>T (COL6A2))

Chromosome 21
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.47552423C>T
DNA change (hg38) g.46132509C>T
Published as COL6A2(NM_001849.3):c.3017C>T (p.(Ala1006Val))
ISCN -
DB-ID COL6A2_000239
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) 0.00045 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.3017C>T r.(?) p.(Ala1006Val)
FTCD NM_006657.2 ?/. - c.*3988G>A r.(=) p.(=)


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