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 ... 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 …
LOVD
WebDYSF gene mutations may disrupt the function of the dysferlin protein and interfere with the muscle repair process. ... Pellissier JF, Pouget J, Hammouda el H, Laforet P, Urtizberea JA, Eymard B, Leturcq F, Levy N. Analysis of the DYSF mutationalspectrum in a large cohort of patients. Hum Mutat. 2009 Feb;30(2):E345-Reprinted from MedlinePlus ... WebDec 1, 2007 · Heterozygous c.4253G A DYSF change was detected in six members of the family (II-2, -4, III-5, -12, -13, and -19) and four homozygous mutations in four individuals including the pa- dr richard ong
[PDF] Mismatch Repair Analysis of Inherited MSH2 and/or
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 http://umd.be/MSH6/4DACTION/WV/568 WebVariation name (cDNA level) Variation name (protein level) Variation status: c.3284G>A: p.Arg1095His dr richard onishi