Variant #0000523585 (NC_000004.11:g.981603dup, IDUA(NM_000203.3):c.165dup)

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.981603dup
DNA change (hg38) g.987815dup
Published as IDUA(NM_000203.5):c.165dupG (p.L56Afs*7)
ISCN -
DB-ID IDUA_000138
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDUA NM_000203.3 +/. - c.165dup r.(?) p.(Leu56AlafsTer7)
SLC26A1 NM_213613.3 +/. - c.*1018dup r.(?) p.(=)