Mutation

Primary Site >> Stomach Cancer

Gene >> UGT1A3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233767858:233767858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139607673
CDS Mutation	c.1009C>T
AA Mutation	p.Arg337Trp(p.R337W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233767880:233767880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144978321
CDS Mutation	c.1031C>T
AA Mutation	p.Ser344Leu(p.S344L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233729433:233729433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307A>G
AA Mutation	p.Thr103Ala(p.T103A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233729443:233729443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317T>G
AA Mutation	p.Phe106Cys(p.F106C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000482026
Start	233767931:233767931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1082T>C
AA Mutation	p.Leu361Pro(p.L361P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482026
Start	233768290:233768290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765390164
CDS Mutation	c.1158C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482026
Start	233729597:233729597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375083511
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000482026
Start	233729169:233729169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770212311
CDS Mutation	c.43G>T
AA Mutation	p.Gly15Ter(p.G15*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000482026
Start	233729844:233729845(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.725_726dupAG
AA Mutation	p.Val243ArgfsTer21(p.V243Rfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000482026
Start	233767848:233767848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript