Colon Cancer: Gene >> MSN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360270
Start	65729600:65729600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355C>A
AA Mutation	p.Pro119Thr(p.P119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360270
Start	65735349:65735349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.878G>A
AA Mutation	p.Arg293His(p.R293H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360270
Start	65731175:65731175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536A>G
AA Mutation	p.His179Arg(p.H179R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360270
Start	65739147:65739147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1522C>T
AA Mutation	p.Arg508Cys(p.R508C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360270
Start	65739133:65739133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1508G>A
AA Mutation	p.Arg503His(p.R503H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360270
Start	65736836:65736836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001A>G
AA Mutation	p.Glu334Gly(p.E334G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360270
Start	65731175:65731175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.536A>T
AA Mutation	p.His179Leu(p.H179L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360270
Start	65729515:65729515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360270
Start	65735296:65735296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360270
Start	65735353:65735353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360270
Start	65735272:65735272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360270
Start	65735356:65735357(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.887dupA
AA Mutation	p.Pro297AlafsTer2(p.P297Afs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MSN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360270
Start	65731875:65731875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589G>T
AA Mutation	p.Asp197Tyr(p.D197Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript