Dysf c.3284g a p.arg1095his
WebEffect: The variant's effect on the function of the gene/protein, displayed in the format 'R/C'. R is the value reported by the source (publication, submitter) and this classification may vary between records. C is the value concluded by the curator. Note that in some database the curator uses Summary records to give details on the ... WebUMD-DYSF c.107_108delAA (3) p.Lys36SerfsX12 2 LGMD2B 1 Miyoshi myopathy 1 Miyoshi myopathy 54 c.265C>T (6) p.Arg89X 4 Miyoshi myopathy 1 Miyoshi myopathy 1 Miyoshi myopathy 22 Miyoshi myopathy 53 Miyoshi myopathy 61 Miyoshi myopathy, atypical 73 c.331C>T (4) p.Gln111X 4 Miyoshi myopathy 1 LGMD2B or Miyoshi myopathy 64
Dysf c.3284g a p.arg1095his
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WebThe role of one of the most frequently reported MMR gene VUS, MSH2 c.380A>G (p.Asn127Ser), is especially interesting because its concomitant defect with another variant could WebFeb 21, 2014 · The UMD-MSH6 mutations database Mutations involving exon 5 Request ID: 14640927506
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WebAug 18, 2024 · Nine patients had extrahepatic manifestations including short stature, skeletal abnormalities, intellectual disability, ophthalmic abnormalities, low levels of … WebThe DYSF gene homepage. This database is one of the gene variant databases from the Leiden Muscular Dystrophy pages. NOTE: the DYSF coding DNA reference sequence …
WebVariant #0000417648 (NC_000002.11:g.48030670G>A, MSH6(NM_000179.2):c.3284G>A) Individual ID: 00204100: Chromosome: 2: Allele: Unknown: Affects function (as reported) Does not affect function: Affects function (by curator) Not classified ... displayed in the format 'R/C'. R is the value reported by the source (publication, submitter) and this ...
WebIn patients with LGMD2B or Miyoshi myopathy, Spuler et al. (2008) identified 3 different mutations in the N terminus of the DYSF gene ( 603009.0017 - 603009.0019) that resulted in deposition of dysferlin-reactive amyloid fibrils within muscle fibers. The authors postulated that amyloid protein is a proteolytic cleavage product of dysferlin, and ... something a cowboy might wearWebNomenclature c. Nomenclature p. Structure: HCD: Conservation: Splice site: Pathogenicity: Conclusion: c.3001A>T: p.Thr1001Ser: Inner DysF domain, N-terminal: Inner ... small chest tattoo ideas for womenWebVariation name (cDNA level) Variation name (protein level) Variation status: c.3284G>A: p.Arg1095His something adjacentWebSep 10, 2024 · Variant summary: MSH6 c.3284G>A (p.Arg1095His) results in a non-conservative amino acid change located in the DNA mismatch repair protein MutS, core … small chests of drawers ukWebBackground: The dysferlin gene or the DYSF gene encodes the Ca 2+-dependent phospholipid-binding protein dysferlin, which belongs to the ferlin family and is associated with muscle membrane regeneration and repair.Variants in the DYSF gene are responsible for limb-girdle muscular dystrophy type 2B (LGMD2B), also called limb-girdle muscular … something addictiveWebDysferlin also known as dystrophy-associated fer-1-like protein is a protein that in humans is encoded by the DYSF gene.. Dysferlin is linked with stabilization of calcium signaling and membrane repair. A defect in the DYSF gene, located on chromosome 2p12-14, results in several types of muscular dystrophy; including Miyoshi myopathy (MM), Limb-girdle … something activehttp://www.umd.be/DYSF/W_DYSF/3001%20to%203500.html something a dog might fetch crossword