Variant #0000346455 (NC_000004.11:g.980971T>G, IDUA(NM_000203.3):c.99T>G)

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.980971T>G
DNA change (hg38) g.987183T>G
Published as IDUA(NM_000203.5):c.99T>G (p.H33Q), SLC26A1(NM_134425.4):c.576+3945A>C
ISCN -
DB-ID IDUA_000088 See all 4 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) 0.8399 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.99T>G r.(?) p.(His33Gln)
SLC26A1 NM_213613.3 -/. - c.*1650A>C r.(=) p.(=)