Colon Cancer: Gene >> GPT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394955
Start	144505307:144505307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557T>C
AA Mutation	p.Ile186Thr(p.I186T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394955
Start	144506400:144506400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1125C>A
AA Mutation	p.Phe375Leu(p.F375L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394955
Start	144506571:144506571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202C>A
AA Mutation	p.Pro401His(p.P401H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394955
Start	144506601:144506601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1232C>T
AA Mutation	p.Ala411Val(p.A411V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394955
Start	144505041:144505041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405C>A
AA Mutation	p.Asp135Glu(p.D135E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394955
Start	144505921:144505921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394955
Start	144504337:144504337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554853278
CDS Mutation	c.33G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394955
Start	144506923:144506923(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1419delC
AA Mutation	p.Leu474TrpfsTer11(p.L474Wfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394955
Start	144506922:144506923(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs776744432
CDS Mutation	c.1419dupC
AA Mutation	p.Glu475GlyfsTer72(p.E475Gfs*72)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GPT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394955
Start	144506621:144506621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777867324
CDS Mutation	c.1252G>A
AA Mutation	p.Val418Met(p.V418M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript