Colon Cancer: Gene >> P2RY6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349767
Start	73297501:73297501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193163379
CDS Mutation	c.983G>A
AA Mutation	p.Arg328His(p.R328H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349767
Start	73296969:73296969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374484031
CDS Mutation	c.451G>A
AA Mutation	p.Val151Met(p.V151M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000349767
Start	73297329:73297329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200512829
CDS Mutation	c.811G>A
AA Mutation	p.Val271Ile(p.V271I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349767
Start	73296742:73296742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224A>G
AA Mutation	p.Tyr75Cys(p.Y75C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000349767
Start	73297500:73297500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773575254
CDS Mutation	c.982C>T
AA Mutation	p.Arg328Cys(p.R328C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000349767
Start	73296816:73296816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574690210
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Cys(p.R100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349767
Start	73297241:73297241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349767
Start	73297232:73297232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.714C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> P2RY6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349767
Start	73296817:73296817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201497467
CDS Mutation	c.299G>A
AA Mutation	p.Arg100His(p.R100H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349767
Start	73296647:73296647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129G>A
Mutation Classification	Silent
Feature Type	Transcript