Variant #0000704906 (NC_000017.10:g.48275131G>A, NM_000088.3:c.658C>T (COL1A1))

Chromosome 17
Allele Maternal (confirmed)
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.48275131G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL1A1_000012 See all 18 reported entries
Variant remarks -
Reference PubMed: Wang et al., 2019
ClinVar ID -
dbSNP ID rs72667036
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Raymond Dalgleish
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Raymond Dalgleish
Date created 2019-08-14 10:42:12 +02:00 (CEST)
Date last edited 2022-01-26 15:37:48 +01:00 (CET)
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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 +/+ 9 c.658C>T r.? p.(Arg220*) nonsense Arg42Stop



Screenings

Stop! No screenings found!


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