Variant #0000289100 (NC_000011.9:g.118963736C>T, NC_000011.9(NM_000190.3):c.912+5C>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.118963736C>T
DNA change (hg38) g.119093026C>T
Published as HMBS(NM_000190.4):c.912+5C>T
ISCN -
DB-ID HMBS_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-01 15:51:35 +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.912+5C>T r.spl? p.?
DPAGT1 NM_001382.3 -?/. - c.*3972G>A r.(=) p.(=)
H2AFX NM_002105.2 -?/. - c.*1937G>A r.(=) p.(=)


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