Primary Site >> Stomach Cancer

Gene >> COG2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000366669
Start 230671613:230671613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199855667
CDS Mutation c.872G>A
AA Mutation p.Arg291Gln(p.R291Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000366669
Start 230678969:230678969(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1083G>T
AA Mutation p.Gln361His(p.Q361H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000366669
Start 230691559:230691559(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140155560
CDS Mutation c.2110G>A
AA Mutation p.Glu704Lys(p.E704K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000366669
Start 230669462:230669462(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.701A>C
AA Mutation p.Tyr234Ser(p.Y234S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000366669
Start 230664515:230664515(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199727575
CDS Mutation c.413G>A
AA Mutation p.Arg138Gln(p.R138Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000366669
Start 230693347:230693347(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2171A>G
AA Mutation p.Glu724Gly(p.E724G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000366669
Start 230659472:230659472(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.81C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000366669
Start 230691483:230691483(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs575955728
CDS Mutation c.2034C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000366669
Start 230683589:230683589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1182G>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000366669
Start 230663213:230663213(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.380delA
AA Mutation p.Lys127ArgfsTer5(p.K127Rfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000366669
Start 230663186:230663186(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.346C>T
AA Mutation p.Arg116Ter(p.R116*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000366669
Start 230669463:230669463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.702C>A
AA Mutation p.Tyr234Ter(p.Y234*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript