Colon Cancer: Gene >> GC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273951
Start	71758070:71758070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803C>T
AA Mutation	p.Ser268Phe(p.S268F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273951
Start	71765606:71765606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299C>A
AA Mutation	p.Ser100Tyr(p.S100Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273951
Start	71758112:71758112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761T>A
AA Mutation	p.Leu254Gln(p.L254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273951
Start	71755087:71755087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055G>A
AA Mutation	p.Arg352Lys(p.R352K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273951
Start	71758072:71758072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801G>T
AA Mutation	p.Glu267Asp(p.E267D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273951
Start	71752530:71752530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273951
Start	71758066:71758066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273951
Start	71769384:71769384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000273951
Start	71768300:71768300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273951
Start	71768324:71768324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746394990
CDS Mutation	c.238G>C
AA Mutation	p.Asp80His(p.D80H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273951
Start	71765473:71765473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273951
Start	71756835:71756836(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.910dupA
AA Mutation	p.Thr304AsnfsTer33(p.T304Nfs*33)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript