Variant #0000979392 (NC_000011.9:g.118968266G>T, NM_000190.3:c.*4273G>T (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.118968266G>T
DNA change (hg38) -
Published as DPAGT1(NM_001382.4):c.918-5C>A
ISCN -
DB-ID DPAGT1_000026
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 2024-04-19 20:27:30 +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.*4273G>T r.(=) p.(=)
DPAGT1 NM_001382.3 ?/. - c.918-5C>A r.spl? p.?
H2AFX NM_002105.2 ?/. - c.-2162C>A r.(?) p.(=)


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