Colon Cancer: Gene >> MAGI3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113683977:113683977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4409T>G
AA Mutation	p.Val1470Gly(p.V1470G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113683190:113683190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3622C>A
AA Mutation	p.Leu1208Ile(p.L1208I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113653950:113653950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2561T>C
AA Mutation	p.Leu854Ser(p.L854S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113683447:113683447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3879A>C
AA Mutation	p.Gln1293His(p.Q1293H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113683626:113683626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4058C>A
AA Mutation	p.Ser1353Tyr(p.S1353Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113585498:113585498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.665G>A
AA Mutation	p.Arg222Gln(p.R222Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113622813:113622813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179A>C
AA Mutation	p.Glu393Asp(p.E393D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113614643:113614643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061G>A
AA Mutation	p.Gly354Glu(p.G354E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113649287:113649287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2206T>C
AA Mutation	p.Phe736Leu(p.F736L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307546
Start	113684005:113684005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4437A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307546
Start	113672648:113672648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2952C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307546
Start	113653846:113653846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760284762
CDS Mutation	c.2457C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307546
Start	113672696:113672696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3000G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307546
Start	113683074:113683074(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3509delA
AA Mutation	p.Lys1170ArgfsTer5(p.K1170Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307546
Start	113683297:113683297(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3734delA
AA Mutation	p.Asn1245IlefsTer65(p.N1245Ifs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000307546
Start	113585591:113585592(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.758_759insTTACTAATGTTG
AA Mutation	p.Asn253_Ala254insTyrTerCysCys(p.N253_A254insY*CC)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000307546
Start	113683616:113683617(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4048_4049insTTTGATG
AA Mutation	p.Arg1350IlefsTer2(p.R1350Ifs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307546
Start	113683894:113683895(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4326_4327insCATTTTCTCCTATTTTATCGTTACT
AA Mutation	p.Arg1443HisfsTer9(p.R1443Hfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307546
Start	113683920:113683921(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4352_4353insT
AA Mutation	p.Val1452SerfsTer2(p.V1452Sfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307546
Start	113683921:113683922(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4353_4354insTTTTATC
AA Mutation	p.Val1452PhefsTer4(p.V1452Ffs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307546
Start	113683633:113683634(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.4072dupA
AA Mutation	p.Ile1358AsnfsTer6(p.I1358Nfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAGI3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113683917:113683917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4349C>A
AA Mutation	p.Ser1450Tyr(p.S1450Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113659151:113659151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2701G>T
AA Mutation	p.Asp901Tyr(p.D901Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113659213:113659213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2763G>T
AA Mutation	p.Gln921His(p.Q921H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307546
Start	113681286:113681286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3278A>C
AA Mutation	p.Asn1093Thr(p.N1093T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript