Variant #0000998809 (NC_000011.9:g.118963677C>A, NM_000190.3:c.858C>A (HMBS))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.118963677C>A
DNA change (hg38) -
Published as HMBS(NM_000190.3):c.858C>A (p.(Asp286Glu))
ISCN -
DB-ID DPAGT1_000028
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMBS NM_000190.3 ?/. - c.858C>A r.(?) p.(Asp286Glu)
DPAGT1 NM_001382.3 ?/. - c.*4031G>T r.(=) p.(=)
H2AFX NM_002105.2 ?/. - c.*1996G>T r.(=) p.(=)


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