Colon Cancer: Gene >> UGT1A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233768291:233768291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143573365
CDS Mutation	c.1159G>A
AA Mutation	p.Val387Ile(p.V387I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233767137:233767137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971C>A
AA Mutation	p.Ala324Asp(p.A324D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233767161:233767161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995A>C
AA Mutation	p.Gln332Pro(p.Q332P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233768289:233768289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Gly386Asp(p.G386D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233729877:233729877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751C>T
AA Mutation	p.His251Tyr(p.H251Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233729342:233729342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368262266
CDS Mutation	c.216G>T
AA Mutation	p.Glu72Asp(p.E72D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000482026
Start	233729311:233729311(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.188delC
AA Mutation	p.Pro63GlnfsTer3(p.P63Qfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000482026
Start	233729337:233729337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211G>T
AA Mutation	p.Glu71Ter(p.E71*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UGT1A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233768343:233768343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140613392
CDS Mutation	c.1211G>A
AA Mutation	p.Arg404His(p.R404H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482026
Start	233729585:233729585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138617806
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript