Colon Cancer: Gene >> PTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348225
Start	137251243:137251243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438G>T
AA Mutation	p.Lys146Asn(p.K146N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348225
Start	137253553:137253553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200G>A
AA Mutation	p.Arg67Gln(p.R67Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348225
Start	137253593:137253593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>T
AA Mutation	p.Val54Leu(p.V54L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348225
Start	137251341:137251341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340G>T
AA Mutation	p.Ala114Ser(p.A114S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000348225
Start	137253630:137253630(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.123delA
AA Mutation	p.Val42Ter(p.V42*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PTN

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000348225
Start	137228073:137228073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454G>A
AA Mutation	p.Glu152Lys(p.E152K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript