Colon Cancer: Gene >> P2RY12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302632
Start	151338710:151338710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.136G>A
AA Mutation	p.Ala46Thr(p.A46T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302632
Start	151338343:151338343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503G>A
AA Mutation	p.Arg168Lys(p.R168K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302632
Start	151338319:151338319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527C>A
AA Mutation	p.Ser176Tyr(p.S176Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302632
Start	151338079:151338079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121917885
CDS Mutation	c.767G>A
AA Mutation	p.Arg256Gln(p.R256Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302632
Start	151338543:151338543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778319065
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302632
Start	151338834:151338834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41267893
CDS Mutation	c.12C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302632
Start	151338204:151338204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.642A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302632
Start	151338795:151338795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302632
Start	151338816:151338816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369115073
CDS Mutation	c.30G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302632
Start	151338566:151338567(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.279_280insG
AA Mutation	p.Thr94AspfsTer38(p.T94Dfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> P2RY12

No Mutation Annotation!