Primary Site >> Stomach Cancer

Gene >> PCGF2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000611883
Start 38738837:38738837(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs554363495
CDS Mutation c.341G>A
AA Mutation p.Arg114His(p.R114H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000611883
Start 38739103:38739103(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780536842
CDS Mutation c.281G>A
AA Mutation p.Arg94Gln(p.R94Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000611883
Start 38740340:38740340(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs191878813
CDS Mutation c.63C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000611883
Start 38739084:38739084(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758029170
CDS Mutation c.300G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000611883
Start 38740334:38740334(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.69delG
AA Mutation p.Tyr24ThrfsTer44(p.Y24Tfs*44)
Mutation Classification Frame_Shift_Del
Feature Type Transcript