Colon Cancer: Gene >> AGT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366667
Start	230706157:230706157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900C>A
AA Mutation	p.Phe300Leu(p.F300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366667
Start	230710544:230710544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307G>A
AA Mutation	p.Ala103Thr(p.A103T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366667
Start	230710439:230710439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412G>A
AA Mutation	p.Ala138Thr(p.A138T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366667
Start	230710840:230710840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61762541
CDS Mutation	c.11G>A
AA Mutation	p.Arg4Gln(p.R4Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366667
Start	230706120:230706120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937C>T
AA Mutation	p.Leu313Phe(p.L313F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366667
Start	230710661:230710661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374540090
CDS Mutation	c.190G>T
AA Mutation	p.Asp64Tyr(p.D64Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366667
Start	230703253:230703253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1346C>A
AA Mutation	p.Pro449His(p.P449H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366667
Start	230710758:230710758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366667
Start	230704208:230704208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366667
Start	230710011:230710011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.840C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000366667
Start	230703308:230703308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780763836
CDS Mutation	c.1291G>T
AA Mutation	p.Glu431Ter(p.E431*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AGT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366667
Start	230710661:230710661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374540090
CDS Mutation	c.190G>T
AA Mutation	p.Asp64Tyr(p.D64Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366667
Start	230705956:230705956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript