Variant #0000972010 (NC_000017.10:g.48275531del, NM_000088.3:c.579del (COL1A1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48275531del
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL1A1_000293 See all 33 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs72667023
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-03-15 18:03:01 +01:00 (CET)
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 +/. - c.579del r.(?) p.(Gly194ValfsTer71) - -


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