Variant #0000875779 (NC_000017.10:g.48266597G>A, NM_000088.3:c.2869C>T (COL1A1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.48266597G>A
DNA change (hg38) g.50189236G>A
Published as -
ISCN -
DB-ID COL1A1_000238 See all 7 reported entries
Variant remarks Nonsense variants are a known pathogenic mechanism in COL1A1
Reference -
ClinVar ID -
dbSNP ID rs72653161
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Gerard Pals
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-08-13 13:51:05 +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     

Predicted     

Legacy protein change     
COL1A1 NM_000088.3 +/. 40 c.2869C>T r.(?) p.(Gln957Ter) - -


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