Variant #0000875821 (NC_000017.10:g.48266137C>G, NM_000088.3:c.3065G>C (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.48266137C>G
DNA change (hg38) g.50188776C>G
Published as -
ISCN -
DB-ID COL1A1_000182 See all 3 reported entries
Variant remarks Substitutions of Gly in the first position of a GlyXY triplet in the triple helix domain will always disrupt triple helix formation and are considered to be pathogenic
Reference -
ClinVar ID -
dbSNP ID rs67771061
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 +/. 42 c.3065G>C r.(?) p.(Gly1022Ala) - -


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