Mutation

Primary Site >> Stomach Cancer

Gene >> ORC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52374820:52374820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767782494
CDS Mutation	c.2381C>T
AA Mutation	p.Thr794Met(p.T794M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52381664:52381664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2111C>T
AA Mutation	p.Ala704Val(p.A704V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52385931:52385931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141623460
CDS Mutation	c.1402C>T
AA Mutation	p.Arg468Cys(p.R468C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52373258:52373258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2509A>G
AA Mutation	p.Ser837Gly(p.S837G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52373345:52373345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2422A>C
AA Mutation	p.Met808Leu(p.M808L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52389271:52389271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378His(p.R378H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52396165:52396165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.602C>T
AA Mutation	p.Ser201Phe(p.S201F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52393735:52393735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181880288
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Trp(p.R264W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52396333:52396333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434C>T
AA Mutation	p.Pro145Leu(p.P145L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371566
Start	52385924:52385924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1409C>T
AA Mutation	p.Ala470Val(p.A470V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371566
Start	52373195:52373195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2572C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371566
Start	52383920:52383920(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1773delA
AA Mutation	p.Ala592GlnfsTer41(p.A592Qfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript