Colon Cancer: Gene >> PTP4A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329397
Start	141422302:141422302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.62T>C
AA Mutation	p.Ile21Thr(p.I21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329397
Start	141425081:141425081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776517948
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Cys(p.R47C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329397
Start	141430980:141430980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458G>A
AA Mutation	p.Arg153Gln(p.R153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329397
Start	141426971:141426971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140695360
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTP4A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329397
Start	141427805:141427805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385G>A
AA Mutation	p.Ala129Thr(p.A129T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000329397
Start	141431025:141431030(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.503_508delCCCGGT
AA Mutation	p.Thr168_Cys170delinsSer(p.T168_C170delinsS)
Mutation Classification	In_Frame_Del
Feature Type	Transcript