Colon Cancer: Gene >> PTGER4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40691921:40691921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010T>G
AA Mutation	p.Leu337Arg(p.L337R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40681310:40681310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317G>A
AA Mutation	p.Gly106Asp(p.G106D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40681373:40681373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380A>G
AA Mutation	p.Tyr127Cys(p.Y127C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40692215:40692215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138674524
CDS Mutation	c.1304G>A
AA Mutation	p.Arg435Gln(p.R435Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40681394:40681394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401G>A
AA Mutation	p.Arg134Gln(p.R134Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40691858:40691858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Arg316Gln(p.R316Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302472
Start	40681449:40681449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302472
Start	40681026:40681026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302472
Start	40681252:40681252(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.263delG
AA Mutation	p.Gly88AlafsTer26(p.G88Afs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PTGER4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302472
Start	40681278:40681278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285C>G
AA Mutation	p.Ser95Arg(p.S95R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript