Full data view for gene HSPB1

This database is one of the gene variant databases from the "Leiden Muscular Dystrophy pages" (LMDp)
Information The variants shown are described using the NM_001540.3 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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.407G>A r.(?) p.(Arg136Gln) Unknown ACMG pathogenic g.75933161G>A g.76303844G>A - - HSPB1_000058 ACMG PM1, PM2, PM5_str, PP2, PP3, PP5 PubMed: Molaei 2025 SCV006074986 - Germline - - - - - DNA SEQ, SEQ-NG - WES neuropathy Fam106689Pat351 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M no Iran - - - - - 1 Johan den Dunnen
+/. 2 c.407G>A r.(?) p.(Arg136Gln) Unknown - pathogenic (dominant) g.75933161G>A g.76303844G>A - - HSPB1_000058 - PubMed: Beecroft 2020 - - Germline/De novo (untested) - - - - - DNA SEQ, SEQ-NG - 336-gene panel MYOP MF145 PubMed: Beecroft 2020 analysis 2249 neurology patients M - (Australia);(New Zealand) - - - - - 1 Johan den Dunnen
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