Variant #0000876067 (NC_000017.10:g.(48277309_48278771)_(48267094_48267219)del, NC_000017.10(NM_000088.3):c.(103+1_104-1)_(2613+1_2614-1)del (COL1A1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(48277309_48278771)_(48267094_48267219)del
DNA change (hg38) g.(50199948_50201410)_(50189733_50189858)del
Published as -
ISCN -
DB-ID COL1A1_000753 See all 2 reported entries
Variant remarks multi-exon deletion with frameshift and NMD
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Gerard Pals
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-08-13 13:51:05 +02:00 (CEST)
Date last edited 2022-08-17 16:32:23 +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 ?/+ 1i_37i c.(103+1_104-1)_(2613+1_2614-1)del r.104_2613del p.0 - -


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