Colon Cancer: Gene >> ESAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278927
Start	124753783:124753783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036A>G
AA Mutation	p.Arg346Gly(p.R346G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278927
Start	124753941:124753941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759294805
CDS Mutation	c.878G>A
AA Mutation	p.Arg293Gln(p.R293Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278927
Start	124754673:124754673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698C>T
AA Mutation	p.Ala233Val(p.A233V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278927
Start	124758393:124758393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202080091
CDS Mutation	c.205C>T
AA Mutation	p.Pro69Ser(p.P69S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278927
Start	124756300:124756300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514C>A
AA Mutation	p.Leu172Met(p.L172M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278927
Start	124762119:124762119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278927
Start	124756575:124756575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749002095
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278927
Start	124753931:124753931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ESAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278927
Start	124753896:124753896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923G>T
AA Mutation	p.Gly308Val(p.G308V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278927
Start	124756585:124756585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407A>C
AA Mutation	p.Lys136Thr(p.K136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript