Colon Cancer: Gene >> PITX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354925
Start	110618334:110618334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745A>C
AA Mutation	p.Ser249Arg(p.S249R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354925
Start	110618252:110618252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.827C>T
AA Mutation	p.Thr276Met(p.T276M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354925
Start	110632350:110632350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752299951
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000354925
Start	110621271:110621271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>T
AA Mutation	p.Gln95Ter(p.Q95*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000354925
Start	110632376:110632376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151A>T
AA Mutation	p.Lys51Ter(p.K51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PITX2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000354925
Start	110621205:110621205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349G>T
AA Mutation	p.Glu117Ter(p.E117*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript