Variant #0000705442 (NC_000017.10:g.48272592C>T, NC_000017.10(NM_000088.3):c.1299+1G>A (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.48272592C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL1A1_000400 See all 38 reported entries
Variant remarks -
Reference PubMed: Zhang et al., 2017
ClinVar ID -
dbSNP ID rs66490707
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Raymond Dalgleish
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Raymond Dalgleish
Date created 2019-08-30 16:50:49 +02:00 (CEST)
Date last edited 2022-01-26 16:22:41 +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 +/+ 19i c.1299+1G>A r.? - splicing affected? -



Screenings

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