Colon Cancer: Gene >> AGTR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116172723:116172723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443A>G
AA Mutation	p.Tyr148Cys(p.Y148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116172830:116172830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782035382
CDS Mutation	c.550G>A
AA Mutation	p.Val184Ile(p.V184I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116172398:116172398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782530337
CDS Mutation	c.118T>A
AA Mutation	p.Ser40Thr(p.S40T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116173269:116173269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782176432
CDS Mutation	c.989G>A
AA Mutation	p.Arg330His(p.R330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116172496:116172496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216A>C
AA Mutation	p.Gln72His(p.Q72H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116173249:116173249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969C>A
AA Mutation	p.Asn323Lys(p.N323K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116172816:116172816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536T>G
AA Mutation	p.Phe179Cys(p.F179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116173217:116173217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782155285
CDS Mutation	c.937G>A
AA Mutation	p.Val313Ile(p.V313I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371906
Start	116172495:116172495(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.218delA
AA Mutation	p.Lys73ArgfsTer43(p.K73Rfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AGTR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116173217:116173217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782155285
CDS Mutation	c.937G>A
AA Mutation	p.Val313Ile(p.V313I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371906
Start	116172744:116172744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464G>T
AA Mutation	p.Arg155Ile(p.R155I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371906
Start	116172340:116172340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782532455
CDS Mutation	c.60C>T
Mutation Classification	Silent
Feature Type	Transcript