Colon Cancer: Gene >> PTPN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309660
Start	12884093:12884093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Cys(p.R17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309660
Start	12836810:12836810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242G>C
AA Mutation	p.Arg81Thr(p.R81T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309660
Start	12859185:12859185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139A>G
AA Mutation	p.Arg47Gly(p.R47G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309660
Start	12830963:12830963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771096169
CDS Mutation	c.340C>T
AA Mutation	p.Arg114Cys(p.R114C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309660
Start	12817278:12817278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583T>C
AA Mutation	p.Phe195Leu(p.F195L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000309660
Start	12817260:12817260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.601G>T
AA Mutation	p.Glu201Ter(p.E201*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000309660
Start	12830942:12830942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PTPN2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309660
Start	12802053:12802053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000309660
Start	12859248:12859248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.76C>T
AA Mutation	p.Arg26Ter(p.R26*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript