Colon Cancer: Gene >> PRRX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372469
Start	129720740:129720740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.592G>T
AA Mutation	p.Asp198Tyr(p.D198Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372469
Start	129720657:129720657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766187907
CDS Mutation	c.509G>A
AA Mutation	p.Arg170His(p.R170H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372469
Start	129719252:129719252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281G>A
AA Mutation	p.Arg94His(p.R94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372469
Start	129720669:129720669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521T>C
AA Mutation	p.Leu174Pro(p.L174P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372469
Start	129719391:129719391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372469
Start	129719373:129719373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749511698
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372469
Start	129720655:129720655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRRX2

No Mutation Annotation!