Colon Cancer: Gene >> PTPN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50579865:50579865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027G>A
AA Mutation	p.Asp343Asn(p.D343N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50561435:50561435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136T>C
AA Mutation	p.Tyr46His(p.Y46H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50579310:50579310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845T>C
AA Mutation	p.Met282Thr(p.M282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50578558:50578558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631G>A
AA Mutation	p.Val211Ile(p.V211I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50581426:50581426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250C>T
AA Mutation	p.Thr417Met(p.T417M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50561441:50561441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142G>T
AA Mutation	p.Asp48Tyr(p.D48Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50579809:50579809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.971G>T
AA Mutation	p.Cys324Phe(p.C324F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50578576:50578576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649G>A
AA Mutation	p.Ala217Thr(p.A217T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371621
Start	50579242:50579242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371621
Start	50581301:50581301(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1130delG
AA Mutation	p.Gly377GlufsTer27(p.G377Efs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PTPN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50574629:50574629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467G>A
AA Mutation	p.Arg156Gln(p.R156Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371621
Start	50574561:50574561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399G>T
AA Mutation	p.Met133Ile(p.M133I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript