Colon Cancer: Gene >> TAAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275216
Start	132645645:132645645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359A>C
AA Mutation	p.Asp120Ala(p.D120A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275216
Start	132645697:132645697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759733834
CDS Mutation	c.307G>A
AA Mutation	p.Asp103Asn(p.D103N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275216
Start	132645856:132645856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148C>T
AA Mutation	p.His50Tyr(p.H50Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275216
Start	132645603:132645603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401A>C
AA Mutation	p.Lys134Thr(p.K134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000275216
Start	132645931:132645931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.73T>C
AA Mutation	p.Ser25Pro(p.S25P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000275216
Start	132645355:132645355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770968548
CDS Mutation	c.649G>A
AA Mutation	p.Ala217Thr(p.A217T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000275216
Start	132645850:132645850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154A>T
AA Mutation	p.Lys52Ter(p.K52*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TAAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275216
Start	132645969:132645969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35C>T
AA Mutation	p.Ser12Phe(p.S12F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript