Variant #0001014761 (NC_000011.9:g.118963750G>A, NC_000011.9(NM_000190.3):c.912+19G>A (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.118963750G>A
DNA change (hg38) -
Published as HMBS(NM_000190.4):c.912+19G>A
ISCN -
DB-ID HMBS_000029 See all 2 reported entries
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) 0.00417 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 21:08:56 +01:00 (CET)
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.912+19G>A r.(=) p.(=)
DPAGT1 NM_001382.3 -?/. - c.*3958C>T r.(=) p.(=)
H2AFX NM_002105.2 -?/. - c.*1923C>T r.(=) p.(=)


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