Variant #0000289092 (NC_000011.9:g.118963113G>C, NC_000011.9(NM_000190.3):c.652-1G>C (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.118963113G>C
DNA change (hg38) g.119092403G>C
Published as HMBS(NM_000190.4):c.652-1G>C
ISCN -
DB-ID HMBS_000019
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-01 15:49:38 +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.652-1G>C r.spl? p.?
DPAGT1 NM_001382.3 +/. - c.*4595C>G r.(=) p.(=)
H2AFX NM_002105.2 +/. - c.*2560C>G r.(=) p.(=)


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