Variant #0000705846 (NC_000017.10:g.48269187G>A, NM_000088.3:c.2089C>T (COL1A1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48269187G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL1A1_000198 See all 16 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs72651642
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Margherita Maioli
Database submission license No license selected
Created by Margherita Maioli
Date created 2017-05-26 14:24:23 +02:00 (CEST)
Date last edited 2022-05-13 16:17:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predicted     

Legacy protein change     
COL1A1 NM_000088.3 +/+ 31 c.2089C>T r.? p.(Arg697*) nonsense Arg519Stop



Screenings

Stop! No screenings found!


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