Variant #0000705987 (NC_000017.10:g.48268222C>T, NM_000088.3:c.2299G>A (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.48268222C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL1A1_000118 See all 55 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs72651658
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Xue Bai
Database submission license No license selected
Created by Xue Bai
Date created 2015-05-23 14:10:32 +02:00 (CEST)
Date last edited 2022-07-25 13:47:23 +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 +/+ 33_34 c.2299G>A r.(?) p.(Gly767Ser) missense Gly589Ser



Screenings

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