Colon Cancer: Gene >> NKX3-1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380871
Start	23681400:23681400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Cys(p.R176C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380871
Start	23681307:23681307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753524833
CDS Mutation	c.619C>T
AA Mutation	p.Arg207Trp(p.R207W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380871
Start	23681586:23681586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759016206
CDS Mutation	c.340C>T
AA Mutation	p.Pro114Ser(p.P114S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380871
Start	23681332:23681332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35675040
CDS Mutation	c.594G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000380871
Start	23681385:23681385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.541C>T
AA Mutation	p.Arg181Ter(p.R181*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000380871
Start	23681556:23681556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370C>T
AA Mutation	p.Gln124Ter(p.Q124*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NKX3-1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380871
Start	23681376:23681376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550C>A
AA Mutation	p.Leu184Ile(p.L184I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript