Variant #0000322542 (NC_000011.9:g.118967888A>C, NM_000190.3:c.*3895A>C (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.118967888A>C
DNA change (hg38) g.119097178A>C
Published as DPAGT1(NM_001382.3):c.1125T>G (p.(His375Gln))
ISCN -
DB-ID DPAGT1_000003
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMBS NM_000190.3 ?/. - c.*3895A>C r.(=) p.(=)
DPAGT1 NM_001382.3 ?/. - c.1125T>G r.(?) p.(His375Gln)
H2AFX NM_002105.2 ?/. - c.-1784T>G r.(?) p.(=)


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