Colon Cancer: Gene >> P2RX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225328
Start	3679689:3679689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188788755
CDS Mutation	c.1160C>T
AA Mutation	p.Pro387Leu(p.P387L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000225328
Start	3679782:3679782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067G>A
AA Mutation	p.Gly356Asp(p.G356D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225328
Start	3691658:3691658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776345541
CDS Mutation	c.274G>A
AA Mutation	p.Val92Ile(p.V92I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225328
Start	3690621:3690621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746704729
CDS Mutation	c.420G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225328
Start	3695931:3695931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775381281
CDS Mutation	c.75G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225328
Start	3679655:3679655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146599669
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225328
Start	3690477:3690478(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.482dupG
AA Mutation	p.Thr162HisfsTer3(p.T162Hfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> P2RX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225328
Start	3691757:3691757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175G>A
AA Mutation	p.Asp59Asn(p.D59N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225328
Start	3689594:3689594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225328
Start	3679625:3679625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201152395
CDS Mutation	c.1224C>T
Mutation Classification	Silent
Feature Type	Transcript