TheUMD-MSH2 mutations database
Large rearrangement: c.1077_1276del (deletion from exon 7 to 7)



Data for this mutation


Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
19_11489_11489-001_11489------
19_16126_16126-001_16126------
19_4269_4269-001_4269-001-----
19_4269_4269-002_4269-002-----
19_4269_4269-003_4269-003-----
19_4269_4269-004_4269-004-----
19_4269_4269-009_4269-009-----
19_4269_4269-012_4269-012-----
19_4269_4269-018_4269-018-----
19_4269_4269-020_4269-020-----
19_4269_4269-023_4269-023-----
19_9665_9665-001_9665-001-----
2_02-DDM3526_20706_20706-----
37_L06.46_3912_46494/4649-----
37_L06.46_5843_55765-----
37_L09.014-E_8992_78820-----
37_L09.014-E_8993_80409-----
4_C95046_---_340-----
5_2008058_P0034715_AAC247-----
8_44265_78430_08-123121EG-----
8_F1611_8076_08-652160-----

Biological significanceDate Comment
Causal21/02/14---



Consequences of the mutation at the protein level

No data available