Variant #0000720050 (NC_000004.11:g.981673G>A, IDUA(NM_000203.3):c.235G>A)

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.981673G>A
DNA change (hg38) -
Published as IDUA(NM_000203.3):c.235G>A (p.(Ala79Thr)), IDUA(NM_000203.5):c.235G>A (p.A79T)
ISCN -
DB-ID IDUA_000094 See all 2 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) 0.00227 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDUA NM_000203.3 -/. - c.235G>A r.(?) p.(Ala79Thr)
SLC26A1 NM_213613.3 -/. - c.*948C>T r.(=) p.(=)