Full data view for gene IDS

SUMMARY records: IDS variants classified following ACMG recommendations
Information The variants shown are described using the NM_000202.5 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 1 c.9_10insT r.[9_10insu,9_10=] p.[Pro4SerfsTer43,Pro4=] Unknown - pathogenic (recessive) g.148586658_148586659insA g.149505128_149505129insA 10insT - IDS_000522 the presence of a low amount of normal transcript (8/30) could not be explained other than by possible RNA-editing; editing studies in 2nd paper PubMed: Lualdi 2010, PubMed: Lualdi 2017 - - De novo - - - - - DNA, RNA RT-PCR, SEQ - - MPS2 H150/Pat3 PubMed: Lualdi 2010, PubMed: Lualdi 2017 2-generation family, 1 affected, unaffected non carrier parents/sister M - Italy - - - - - 1 Johan den Dunnen
+/. 1 c.9_10insT r.(?) p.(Pro4SerfsTer43) Unknown ACMG pathogenic (recessive) g.148586658_148586659insA g.149505128_149505129insA - - IDS_000522 - PubMed: Zanetti 2024 SCV005089023 - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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