Variant #0000874929 (NC_000017.10:g.48278770A>G, NC_000017.10(NM_000088.3):c.103+2T>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.48278770A>G
DNA change (hg38) g.50201409A>G
Published as -
ISCN -
DB-ID COL1A1_001054 See all 3 reported entries
Variant remarks Loss of canonical splice donor site. All possible effects are pathogenic in COL1A1
Reference -
ClinVar ID -
dbSNP ID -
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 +/. 1i c.103+2T>C r.spl p.? - -


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