Colon Cancer: Gene >> SERPINE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223095
Start	101135732:101135732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760569885
CDS Mutation	c.1018G>A
AA Mutation	p.Val340Ile(p.V340I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223095
Start	101135771:101135771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774647903
CDS Mutation	c.1057G>A
AA Mutation	p.Glu353Lys(p.E353K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223095
Start	101130432:101130432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Ala95Thr(p.A95T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223095
Start	101135742:101135742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138483939
CDS Mutation	c.1028C>T
AA Mutation	p.Ala343Val(p.A343V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000223095
Start	101128584:101128584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758271488
CDS Mutation	c.191C>T
AA Mutation	p.Ser64Leu(p.S64L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000223095
Start	101130610:101130610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461G>T
AA Mutation	p.Arg154Ile(p.R154I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000223095
Start	101132041:101132041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.672G>A
AA Mutation	p.Met224Ile(p.M224I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223095
Start	101130461:101130461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.312G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223095
Start	101130434:101130434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223095
Start	101133708:101133708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764294088
CDS Mutation	c.714G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223095
Start	101128616:101128616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764559730
CDS Mutation	c.223G>A
AA Mutation	p.Gly75Arg(p.G75R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000223095
Start	101133793:101133793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.799G>T
AA Mutation	p.Glu267Ter(p.E267*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000223095
Start	101128619:101128619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226G>T
AA Mutation	p.Glu76Ter(p.E76*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript