Variant #0000289386 (NC_000004.11:g.980918_980929del, IDUA(NM_000203.3):c.46_57del)

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.980918_980929del
DNA change (hg38) g.987130_987141del
Published as IDUA(NM_000203.5):c.46_57delTCGCTCCTGGCC (p.S16_A19del)
ISCN -
DB-ID IDUA_000003 See all 7 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) Retrieve
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDUA NM_000203.3 +/. - c.46_57del r.(?) p.(Ser16_Ala19del)
SLC26A1 NM_213613.3 +/. - c.*1703_*1714del r.(=) p.(=)