Colon Cancer: Gene >> TAS1R1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6576962:6576962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486G>A
AA Mutation	p.Val496Met(p.V496M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6574893:6574893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761A>G
AA Mutation	p.Glu254Gly(p.E254G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6579120:6579120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2062G>A
AA Mutation	p.Ala688Thr(p.A688T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6578908:6578908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1850G>A
AA Mutation	p.Gly617Asp(p.G617D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6579045:6579045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1987T>C
AA Mutation	p.Ser663Pro(p.S663P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6579336:6579336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2278A>G
AA Mutation	p.Lys760Glu(p.K760E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6571207:6571207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371838719
CDS Mutation	c.490G>A
AA Mutation	p.Val164Met(p.V164M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6555401:6555401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769265487
CDS Mutation	c.28G>A
AA Mutation	p.Gly10Ser(p.G10S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6579013:6579013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149418903
CDS Mutation	c.1955G>A
AA Mutation	p.Arg652His(p.R652H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6579340:6579340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2282G>T
AA Mutation	p.Cys761Phe(p.C761F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6579537:6579537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2479T>G
AA Mutation	p.Phe827Val(p.F827V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333172
Start	6576528:6576528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333172
Start	6578796:6578796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333172
Start	6578750:6578750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1692G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000333172
Start	6577071:6577071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1594+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TAS1R1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333172
Start	6576599:6576599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1445A>C
AA Mutation	p.Lys482Thr(p.K482T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript