Variant #0000862337 (NC_000011.9:g.118963677C>T, NM_000190.3:c.858C>T (HMBS))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.118963677C>T
DNA change (hg38) -
Published as HMBS(NM_000190.4):c.858C>T (p.D286=)
ISCN -
DB-ID DPAGT1_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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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>T r.(?) p.(Asp286=)
DPAGT1 NM_001382.3 -?/. - c.*4031G>A r.(=) p.(=)
H2AFX NM_002105.2 -?/. - c.*1996G>A r.(=) p.(=)


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