Variant #0000989995 (NC_000021.8:g.47531890C>T, NC_000021.8(NM_001849.3):c.116-3C>T (COL6A2))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47531890C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL6A2_000527
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs767597831
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-21 12:18:01 +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.116-3C>T r.(?) p.(?)


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