Colon Cancer: Gene >> DKK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326932
Start	12008401:12008401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182C>T
AA Mutation	p.Thr61Met(p.T61M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326932
Start	11968409:11968409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377759604
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Trp(p.R172W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326932
Start	11968484:11968484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439T>C
AA Mutation	p.Cys147Arg(p.C147R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326932
Start	11964564:11964564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756280059
CDS Mutation	c.953G>A
AA Mutation	p.Arg318His(p.R318H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326932
Start	11998756:11998756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.375A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000326932
Start	11998703:11998705(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.426_428delAAG
AA Mutation	p.Arg143del(p.R143del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DKK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326932
Start	11964508:11964508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009C>T
AA Mutation	p.Pro337Ser(p.P337S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000326932
Start	11966960:11966960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.667C>T
AA Mutation	p.Gln223Ter(p.Q223*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript