Variant #0000984049 (NC_000021.8:g.47552341G>A, NM_001849.3:c.2935G>A (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.47552341G>A
DNA change (hg38) -
Published as COL6A2(NM_001849.3):c.2935G>A (p.D979N), COL6A2(NM_001849.4):c.2935G>A (p.(Asp979Asn))
ISCN -
DB-ID COL6A2_000415 See all 6 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) 0.00019 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 2024-04-19 20:27:30 +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     
COL6A2 NM_001849.3 ?/. - c.2935G>A r.(?) p.(Asp979Asn)
FTCD NM_006657.2 ?/. - c.*4070C>T r.(=) p.(=)


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