TheUMD-MSH2 mutations database
Large rearrangement: c.1_1076del (deletion from exon 1 to 6)



Data for this mutation


Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
19_12059_12059-001_12059------
19_12812_12812-001_12812------
19_15868_15868-001_15868------
19_4330_4330-001_4330-001-----
19_4330_4330-003_4330-003-----
19_4696_4696-002_4696-002-----
19_4696_4696-003_4696-003-----
19_5940_5940-001_5940-001-----
19_5940_5940-002_5940-002-----
37_L03.20_1733_15809-----
37_L05.07_3199_34350-----
37_L13.157-E24921149957-----
37_L13.17225274151696-----
37_L13.17228079161012-----
37_L13.17228080161013-----
37_L13.17228082161015-----
37_L14.15427635162051-----
37_L99.02_1038_5378-----
37_L99.02_265_199-----
4_Di0902_22790_2682-----
5_20122542012002898AAG533-----
SO_-2778---G02622-----

Biological significanceDate Comment
Causal21/02/14---



Consequences of the mutation at the protein level

No data available