Colon Cancer: Gene >> P2RY2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311131
Start	73234833:73234833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674T>C
AA Mutation	p.Leu225Pro(p.L225P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311131
Start	73234407:73234407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248C>T
AA Mutation	p.Ala83Val(p.A83V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311131
Start	73234980:73234980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821T>A
AA Mutation	p.Leu274Gln(p.L274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311131
Start	73234922:73234922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763G>A
AA Mutation	p.Ala255Thr(p.A255T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311131
Start	73234688:73234688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Cys(p.R177C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311131
Start	73234602:73234602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443G>A
AA Mutation	p.Arg148His(p.R148H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311131
Start	73234689:73234689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148967472
CDS Mutation	c.530G>A
AA Mutation	p.Arg177His(p.R177H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311131
Start	73234587:73234587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428G>A
AA Mutation	p.Arg143His(p.R143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311131
Start	73234849:73234849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311131
Start	73234861:73234861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112107964
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311131
Start	73234279:73234279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311131
Start	73234744:73234744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311131
Start	73235005:73235005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> P2RY2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311131
Start	73234340:73234340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Cys(p.R61C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript