Colon Cancer: Gene >> PTGS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186674430:186674430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1738A>G
AA Mutation	p.Asn580Asp(p.N580D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186676154:186676154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001A>G
AA Mutation	p.Tyr334Cys(p.Y334C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186679155:186679155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216C>A
AA Mutation	p.Asn72Lys(p.N72K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186674420:186674420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748C>A
AA Mutation	p.Ser583Tyr(p.S583Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186676864:186676864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>A
AA Mutation	p.Arg231His(p.R231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186674676:186674676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1492C>G
AA Mutation	p.Pro498Ala(p.P498A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186674409:186674409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3218625
CDS Mutation	c.1759G>A
AA Mutation	p.Gly587Arg(p.G587R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186676146:186676146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009C>T
AA Mutation	p.His337Tyr(p.H337Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367468
Start	186680264:186680264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367468
Start	186676540:186676540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201011990
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367468
Start	186679356:186679356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000367468
Start	186679088:186679088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Ter(p.R95*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PTGS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186679087:186679087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200132172
CDS Mutation	c.284G>A
AA Mutation	p.Arg95Gln(p.R95Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186674513:186674513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655C>A
AA Mutation	p.Ser552Tyr(p.S552Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367468
Start	186676071:186676071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084C>T
AA Mutation	p.Arg362Cys(p.R362C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367468
Start	186676120:186676120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367468
Start	186677766:186677766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522C>A
Mutation Classification	Silent
Feature Type	Transcript