Colon Cancer: Gene >> ESD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378720
Start	46782756:46782756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292G>C
AA Mutation	p.Asp98His(p.D98H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378720
Start	46777584:46777584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640T>G
AA Mutation	p.Ser214Ala(p.S214A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378720
Start	46787072:46787072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106T>G
AA Mutation	p.Leu36Val(p.L36V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378720
Start	46791363:46791363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51A>C
AA Mutation	p.Lys17Asn(p.K17N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378720
Start	46791364:46791364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50A>G
AA Mutation	p.Lys17Arg(p.K17R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378720
Start	46781556:46781556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378720
Start	46784295:46784295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378720
Start	46781559:46781559(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.438delT
AA Mutation	p.Phe146LeufsTer11(p.F146Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ESD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378720
Start	46771483:46771483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782G>A
AA Mutation	p.Ser261Asn(p.S261N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000378720
Start	46791421:46791421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-7-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript