Colon Cancer: Gene >> P4HTM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383729
Start	49001456:49001456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455C>G
AA Mutation	p.Thr152Ser(p.T152S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383729
Start	49002570:49002570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698C>T
AA Mutation	p.Ala233Val(p.A233V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383729
Start	49006741:49006741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343G>A
AA Mutation	p.Arg448His(p.R448H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383729
Start	49001530:49001530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529G>A
AA Mutation	p.Glu177Lys(p.E177K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> P4HTM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383729
Start	49006101:49006101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202G>A
AA Mutation	p.Arg401Gln(p.R401Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383729
Start	49004942:49004942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969C>G
Mutation Classification	Silent
Feature Type	Transcript