All variants in the MTM1 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_000252.2 transcript reference sequence.

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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     
+/. 6 c.377_378insT r.(?) p.(Glu126Aspfs*10) - pathogenic g.149787545_149787546insT g.150619072_150619073insT 377insT - MTM1_000058 de novo, in patient (maternal allele) PubMed: Biancalana 2003 - - De novo - - - - - Jorge Oliveira
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