Full data view for gene SBF2

This database is one of the gene variant databases from the Leiden Muscular Dystrophy pages
Information The variants shown are described using the NM_030962.3 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     

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VIP     

Data_av     

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Panel size     

Owner     
+/. 14i c.1601-2A>G r.1601_1617del p.Val534Glyfs*23 Paternal (confirmed) - pathogenic (recessive) g.9985431T>C g.9963884T>C - - SBF2_000091 - PubMed: Lassuthova 2018 - - Germline - - - - - DNA, RNA RT-PCR, SEQ - - CMT FamFPatII:1 PubMed: Lassuthova 2018 2-generation family, 1 affected, unaffected heterozygous carrier father/non-carrier mother M no Czech Republic - >35y - - - 1 Sarah El-Bestawi
+?/. - c.1601-2A>G r.spl p.? Both (homozygous) ACMG likely pathogenic g.9985431T>C g.9963884T>C - - SBF2_000091 ACMG PVS1_VS, PM2 PubMed: Molaei 2025 SCV006075219 - Germline - - - - - DNA SEQ, SEQ-NG - WES CMT Fam103098Pat298 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - 1 Johan den Dunnen
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