Colon Cancer: Gene >> PRDX6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340385
Start	173485502:173485502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Cys(p.R132C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340385
Start	173485422:173485422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314A>G
AA Mutation	p.Asp105Gly(p.D105G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340385
Start	173485479:173485479(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.374delA
AA Mutation	p.Lys125ArgfsTer5(p.K125Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	start_lost
Transcription ID	ENST00000340385
Start	173477398:173477398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PRDX6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340385
Start	173486336:173486336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481C>A
AA Mutation	p.Leu161Ile(p.L161I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340385
Start	173486306:173486306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>A
AA Mutation	p.Ala151Thr(p.A151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340385
Start	173485390:173485390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779663146
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript