Colon Cancer: Gene >> DTL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212078216:212078216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1079C>A
AA Mutation	p.Ser360Tyr(p.S360Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212100942:212100942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1952G>A
AA Mutation	p.Gly651Asp(p.G651D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212100324:212100324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557946653
CDS Mutation	c.1334C>T
AA Mutation	p.Pro445Leu(p.P445L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212078237:212078237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100G>A
AA Mutation	p.Cys367Tyr(p.C367Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212044711:212044711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230G>A
AA Mutation	p.Arg77Gln(p.R77Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212100777:212100777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1787A>C
AA Mutation	p.Glu596Ala(p.E596A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212080660:212080660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171A>G
AA Mutation	p.Asn391Asp(p.N391D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366991
Start	212100262:212100262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1272G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366991
Start	212100403:212100403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1413C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366991
Start	212100766:212100766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1776T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366991
Start	212100403:212100403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1413C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366991
Start	212080644:212080644(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1159delA
AA Mutation	p.Ile387SerfsTer4(p.I387Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000366991
Start	212062949:212062949(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.526+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DTL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212100744:212100744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1754A>G
AA Mutation	p.His585Arg(p.H585R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript