Colon Cancer: Gene >> DMTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265800
Start	22067659:22067659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534685259
CDS Mutation	c.226G>A
AA Mutation	p.Val76Met(p.V76M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265800
Start	22080215:22080215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871C>T
AA Mutation	p.Pro291Ser(p.P291S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265800
Start	22070318:22070318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767628320
CDS Mutation	c.588G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265800
Start	22067601:22067601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761947142
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265800
Start	22069041:22069041(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.281delC
AA Mutation	p.Pro94HisfsTer137(p.P94Hfs*137)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265800
Start	22069483:22069483(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.364delC
AA Mutation	p.Arg122GlyfsTer109(p.R122Gfs*109)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265800
Start	22080821:22080821(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.978delG
AA Mutation	p.Arg327GlyfsTer22(p.R327Gfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265800
Start	22069040:22069041(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs772208110
CDS Mutation	c.281dupC
AA Mutation	p.Pro95ThrfsTer38(p.P95Tfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DMTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265800
Start	22067564:22067564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131T>C
AA Mutation	p.Leu44Pro(p.L44P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265800
Start	22070291:22070291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148314902
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript