Variant #0001029382 (NC_000011.9:g.118963192_118963193del, NM_000190.3:c.730_731del (HMBS))

Chromosome 11
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.118963192_118963193del
DNA change (hg38) -
Published as -
ISCN -
DB-ID DPAGT1_000016 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1565757839
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 2025-02-17 10:46:02 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMBS NM_000190.3 +/. - c.730_731del r.(?) p.(Leu244AlafsTer6)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.