Colon Cancer: Gene >> PTGR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309195
Start	111574801:111574801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693G>T
AA Mutation	p.Lys231Asn(p.K231N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309195
Start	111594247:111594247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127T>C
AA Mutation	p.Phe43Leu(p.F43L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309195
Start	111586086:111586086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289T>C
AA Mutation	p.Ser97Pro(p.S97P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309195
Start	111597415:111597415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776877398
CDS Mutation	c.8G>A
AA Mutation	p.Arg3His(p.R3H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309195
Start	111586006:111586006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309195
Start	111586096:111586096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368370000
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309195
Start	111578880:111578880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745307158
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309195
Start	111592940:111592940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.195G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309195
Start	111597342:111597342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTGR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309195
Start	111570196:111570196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774G>T
AA Mutation	p.Glu258Asp(p.E258D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309195
Start	111574811:111574811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683G>A
AA Mutation	p.Gly228Asp(p.G228D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript