Primary Site >> Stomach Cancer

Gene >> PHACTR4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000373839
Start 28474127:28474127(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1397C>T
AA Mutation p.Pro466Leu(p.P466L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000373839
Start 28466582:28466582(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.637G>A
AA Mutation p.Ala213Thr(p.A213T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000373839
Start 28480604:28480604(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1760G>C
AA Mutation p.Arg587Pro(p.R587P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000373839
Start 28493054:28493054(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2056G>A
AA Mutation p.Glu686Lys(p.E686K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000373839
Start 28474070:28474070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1340A>T
AA Mutation p.Glu447Val(p.E447V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000373839
Start 28476278:28476278(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1593T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000373839
Start 28491760:28491760(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1989T>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000373839
Start 28466682:28466682(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.740delC
AA Mutation p.Pro247GlnfsTer35(p.P247Qfs*35)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000373839
Start 28473761:28473761(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1037delC
AA Mutation p.Pro346HisfsTer33(p.P346Hfs*33)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000373839
Start 28493045:28493045(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2050delA
AA Mutation p.Ser684AlafsTer24(p.S684Afs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript