Colon Cancer: Gene >> GPX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389614
Start	64939672:64939672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389C>A
AA Mutation	p.Pro130Gln(p.P130Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389614
Start	64939576:64939576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485A>T
AA Mutation	p.Glu162Val(p.E162V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389614
Start	64939550:64939550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511C>A
AA Mutation	p.Arg171Ser(p.R171S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389614
Start	64939605:64939605(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773382437
CDS Mutation	c.456delG
AA Mutation	p.Trp152Ter(p.W152*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GPX2

No Mutation Annotation!