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     
+/. - c.122T>C r.(?) p.(Leu41Pro) Both (homozygous) - pathogenic (recessive) g.148585805A>G g.149504275A>G 246T>C - IDS_000288 father not available, deletion excluded PubMed: Cudry 2000 - - Germline - - - - X-inactivation 1.00 skewed DNA, RNA RT-PCR, SEQ - - MPS Pat1 PubMed: Cudry 2000 2-generation family, 1 affected, unaffected carrier mother F - France gypsy - - - - 1 Johan den Dunnen
+?/. 2 c.122T>C r.(?) p.(Leu41Pro) Unknown ACMG likely pathogenic (recessive) g.148585805A>G g.149504275A>G - - IDS_000288 One patient is female (Cudry et al., 2000) PubMed: Zanetti 2024 SCV005089177 - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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