All variants in the SGCB gene

This database is one of the gene variant databases from the Leiden Muscular Dystrophy pages
Information The variants shown are described using the NM_000232.4 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

Owner     
?/. 3 c.392G>A r.(?) p.(Arg131Gln) - VUS g.52895881C>T g.52029715C>T - - SGCB_000116 Sequencing unsuccessful for ~13% of exons (no second variant) PubMed: Nallamilli 2018 - - Germline - - - 0 - Madhuri Hegde
?/. 3 c.392G>A r.(?) p.(Arg131Gln) - VUS g.52895881C>T g.52029715C>T - - SGCB_000116 no second variant PubMed: Nallamilli 2018 - - Germline - - - 0 - Madhuri Hegde
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