Variant #0000542640 (NC_000011.9:g.118963186_118963205dup, NM_000190.3:c.724_743dup (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.118963186_118963205dup
DNA change (hg38) g.119092476_119092495dup
Published as HMBS(NM_000190.4):c.724_743dupGAGACTCTGCTTCGCTGCAT (p.I248Mfs*14)
ISCN -
DB-ID DPAGT1_000008
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-01 15:50:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMBS NM_000190.3 +/. - c.724_743dup r.(?) p.(Ile248MetfsTer14)
DPAGT1 NM_001382.3 +/. - c.*4503_*4522dup r.(=) p.(=)
H2AFX NM_002105.2 +/. - c.*2468_*2487dup r.(=) p.(=)


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