Colon Cancer: Gene >> PRG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311862
Start	57389247:57389247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129G>T
AA Mutation	p.Glu43Asp(p.E43D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311862
Start	57387852:57387852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512G>A
AA Mutation	p.Arg171His(p.R171H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311862
Start	57389265:57389265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111G>T
AA Mutation	p.Glu37Asp(p.E37D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311862
Start	57387816:57387816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753507153
CDS Mutation	c.548C>T
AA Mutation	p.Ala183Val(p.A183V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311862
Start	57388624:57388624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369365761
CDS Mutation	c.451G>A
AA Mutation	p.Ala151Thr(p.A151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311862
Start	57389262:57389262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.114T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311862
Start	57389219:57389219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Glu53Lys(p.E53K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311862
Start	57389908:57389908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37G>A
AA Mutation	p.Ala13Thr(p.A13T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript