Colon Cancer: Gene >> DKK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106924045:106924045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539488952
CDS Mutation	c.689G>A
AA Mutation	p.Arg230His(p.R230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106924692:106924692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.382A>T
AA Mutation	p.Ile128Phe(p.I128F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	107035399:107035399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193G>A
AA Mutation	p.Gly65Ser(p.G65S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106924141:106924141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593A>G
AA Mutation	p.His198Arg(p.H198R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106924046:106924046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761402051
CDS Mutation	c.688C>T
AA Mutation	p.Arg230Cys(p.R230C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106924144:106924144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771137309
CDS Mutation	c.590G>A
AA Mutation	p.Arg197His(p.R197H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106925811:106925811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Cys(p.R121C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	107035464:107035464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128G>A
AA Mutation	p.Gly43Asp(p.G43D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106924638:106924638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565067628
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Trp(p.R146W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106924561:106924561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513G>T
AA Mutation	p.Lys171Asn(p.K171N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	107035534:107035534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58G>C
AA Mutation	p.Val20Leu(p.V20L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285311
Start	106924690:106924690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285311
Start	106924110:106924110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285311
Start	106925878:106925878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000285311
Start	106924556:106924556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518C>A
AA Mutation	p.Ser173Ter(p.S173*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DKK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106924688:106924688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386C>T
AA Mutation	p.Pro129Leu(p.P129L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285311
Start	106924172:106924172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>T
AA Mutation	p.Asp188Tyr(p.D188Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript