Colon Cancer: Gene >> NKX2-1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000498187
Start	36517834:36517834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560C>T
AA Mutation	p.Ser187Leu(p.S187L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000498187
Start	36517912:36517912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482G>A
AA Mutation	p.Arg161His(p.R161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000498187
Start	36517354:36517354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040T>C
AA Mutation	p.Leu347Pro(p.L347P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000498187
Start	36519329:36519329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29C>T
AA Mutation	p.Pro10Leu(p.P10L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000498187
Start	36517742:36517742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652C>T
AA Mutation	p.Arg218Cys(p.R218C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498187
Start	36517398:36517398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746934283
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000498187
Start	36517689:36517689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NKX2-1

No Mutation Annotation!