Colon Cancer: Gene >> PTGS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362012
Start	122377977:122377977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173G>A
AA Mutation	p.Cys58Tyr(p.C58Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362012
Start	122378868:122378868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs10306140
CDS Mutation	c.446G>A
AA Mutation	p.Arg149His(p.R149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362012
Start	122377962:122377962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3842789
CDS Mutation	c.158G>A
AA Mutation	p.Arg53His(p.R53H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362012
Start	122386469:122386469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033G>A
AA Mutation	p.Glu345Lys(p.E345K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000362012
Start	122377998:122377998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194G>A
AA Mutation	p.Gly65Asp(p.G65D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000362012
Start	122383663:122383663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs60893133
CDS Mutation	c.917G>A
AA Mutation	p.Arg306His(p.R306H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000362012
Start	122386560:122386560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124G>A
AA Mutation	p.Arg375His(p.R375H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362012
Start	122392301:122392301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1557G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362012
Start	122377945:122377945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362012
Start	122378503:122378503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201416961
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362012
Start	122392394:122392394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201417140
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362012
Start	122381540:122381540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000362012
Start	122378798:122378798(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs779702921
CDS Mutation	c.381delC
AA Mutation	p.Thr128ProfsTer17(p.T128Pfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PTGS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362012
Start	122392366:122392366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753219685
CDS Mutation	c.1622C>T
AA Mutation	p.Pro541Leu(p.P541L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362012
Start	122377921:122377921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.117A>G
Mutation Classification	Silent
Feature Type	Transcript