TheUMD-APC mutations database
Large rearrangement: c.1_8532del (deletion from exon 1 to 15)



Data for this mutation


Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDAPCMLH1MSH2MSH6MUTYH
10_APC-013---170P-----
10_APC-013---171P-----
10_APC-013---172P-----
10_APC-013---216P-----
10_APC-013---43P-----
10_APC-013---46P-----
10_APC-013---47P-----
10_APC-013---48P-----
10_APC-013---49P-----
10_APC-013---50P-----
10_APC-013---52P-----
10_APC-013---56P-----
10_APC-013---62P-----
10_APC-013---63P-----
10_APC-019---116P-----
10_APC-019---117P-----
10_APC-055---662P-----
10_APC-096---1128P-----
10_APC-096---1186P-----
10_APC-167---2230 P-----
10_APC-198---3037 P-----
10_APC-47---2349 P-----
10_APC141---1726P-----
19_12154---12154.001-----
33_PSL1093---07-534-----
33_PSL2009---08-1558-----
33_PSL2009---10-1723-----
33_PSL2075---08-1741-----
33_PSL821---06-1166-----
37_P01.01-E842--------
37_P01.01-E859--------
37_P12.2120734133184/133185-----
37_P97.011212--------
37_P97.011213--------
37_P97.01355--------
37_P99.01229--------
37_P99.012678--------
37_P99.01829--------
4_19457---19457-----
4_19457---42934-----
4_19457---45210-----
4_28076---28076-----
4_36558---36558-----
7_-1795905283E092227-----
7_-1795ILP0511410E050888-----
7_-1795ILP0511411E050889-----
7_-1795ILP0511542E050991-----
7_-1848ILP0710439E070719-----
7_-517ILP0513178E060044-----
7_-517ILP0711658E072061-----
7_120251011334E101323-----
SO-21-----------
SO_-122444444-----
SO_-122445445-----
SO_-122448448-----
SO_-1244G00549G00549-----
SO_-1456G00021G00021-----
SO_-1456G00426G00426-----
SO_-1456G00431G00431-----
SO_-1456G00479G00479-----
SO_-1456G00480G00480-----
SO_-1456G00484G00484-----
SO_-1456G00485G00485-----
SO_-1456G00539G00539-----
SO_-1456G00600G00600-----
SO_-1456G01934G01934-----
SO_-1469G00004G00004-----
SO_-154G01396G01396-----
SO_-154G01576G01576-----
SO_-154G01859G01859-----
SO_-154G01860G01860-----
SO_-162G05711G05711-----
SO_-1695G00161G00161-----
SO_-1698G00152G00152-----
SO_-1795G00477G00477-----
SO_-1795G00478G00478-----
SO_-279G05269G05269-----
SO_-279GB6180GB6180-----
SO_-31235293529-----
SO_-31236163616-----
SO_-312772772-----
SO_-312G05675G05675-----
SO_-3168G03339G03339-----
SO_-3671G05016G05016-----
SO_-376908908-----
SO_-376909909-----
SO_-376911911-----
SO_-4182G06209G06209-----
SO_-4650125125-----
SO_-4650140140-----
SO_-465075887588-----
SO_-465075977597-----
SO_-465076017601-----
SO_-465076737673-----
SO_-4650G05690G05690-----
SO_-4650G05828G05828-----
SO_-4650G07046G07046-----
SO_-4650G07601G07601-----
SO_-4650G08152G08152-----
SO_-4650G08153G08153-----
SO_-465G01603G01603-----
SO_-497G01619G01619-----
SO_-497G04279G04279-----
SO_-51745784578-----
SO_-51745824582-----
SO_-51745844584-----
SO_-517G01628G01628-----
SO_-61279279-----
SO_-61G05700G05700-----
SO_-787G01047G01047-----
SO_-787G01048G01048-----
SO_-787G01382G01382-----
SO_-787G08067G08067-----
SO_-85356356-----
SO_-8536003600-----
SO_-855G00984G00984-----

Biological significanceDate Comment
Causal28/05/14---



Consequences of the mutation at the protein level

No data available