Colon Cancer: Gene >> WNT10B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301061
Start	48968142:48968142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.515G>T
AA Mutation	p.Ser172Ile(p.S172I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301061
Start	48966418:48966418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766001857
CDS Mutation	c.847A>G
AA Mutation	p.Ile283Val(p.I283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301061
Start	48966312:48966312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.953G>A
AA Mutation	p.Cys318Tyr(p.C318Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301061
Start	48966429:48966429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836T>C
AA Mutation	p.Leu279Pro(p.L279P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000301061
Start	48966307:48966307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958C>T
AA Mutation	p.Arg320Ter(p.R320*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000301061
Start	48967975:48967975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149890665
CDS Mutation	c.682C>T
AA Mutation	p.Arg228Ter(p.R228*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> WNT10B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301061
Start	48968046:48968046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611A>G
AA Mutation	p.Asp204Gly(p.D204G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000301061
Start	48968311:48968311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346G>T
AA Mutation	p.Glu116Ter(p.E116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript