Primary Site >> Stomach Cancer

Gene >> EPHX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000272167
Start 225838702:225838702(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.413G>A
AA Mutation p.Gly138Asp(p.G138D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000272167
Start 225831915:225831915(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.320T>C
AA Mutation p.Val107Ala(p.V107A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000272167
Start 225842457:225842457(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1023G>T
AA Mutation p.Glu341Asp(p.E341D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000272167
Start 225839929:225839929(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs35073925
CDS Mutation c.823A>G
AA Mutation p.Thr275Ala(p.T275A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000272167
Start 225844623:225844623(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755904769
CDS Mutation c.1166G>A
AA Mutation p.Arg389Gln(p.R389Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000272167
Start 225828875:225828875(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.146G>A
AA Mutation p.Arg49His(p.R49H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000272167
Start 225838683:225838683(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs764460024
CDS Mutation c.400delC
AA Mutation p.Gln134SerfsTer12(p.Q134Sfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000272167
Start 225844497:225844497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1041-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
ID 9
Mutation Consequence splice_donor_variant
Transcription ID ENST00000272167
Start 225842476:225842476(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1040+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 10
Mutation Consequence inframe_deletion
Transcription ID ENST00000272167
Start 225838751:225838762(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.462_473delCTACGAGTTTTA
AA Mutation p.Tyr155_Tyr158del(p.Y155_Y158del)
Mutation Classification In_Frame_Del
Feature Type Transcript