Variant #0000801761 (NC_000004.11:g.980908G>T, IDUA(NM_000203.3):c.36G>T)

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.980908G>T
DNA change (hg38) -
Published as IDUA(NM_000203.5):c.36G>T (p.A12=)
ISCN -
DB-ID IDUA_000180
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDUA NM_000203.3 -?/. - c.36G>T r.(?) p.(Ala12=)
SLC26A1 NM_213613.3 -?/. - c.*1713C>A r.(=) p.(=)