Primary Site >> Stomach Cancer

Gene >> FHL2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000322142
Start 105386443:105386443(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.74G>T
AA Mutation p.Ser25Ile(p.S25I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000322142
Start 105363351:105363351(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.622T>C
AA Mutation p.Tyr208His(p.Y208H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000322142
Start 105367680:105367680(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs397517959
CDS Mutation c.391C>A
AA Mutation p.Arg131Ser(p.R131S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000322142
Start 105363366:105363366(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.607C>T
AA Mutation p.Arg203Cys(p.R203C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000322142
Start 105373666:105373666(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.224T>C
AA Mutation p.Leu75Pro(p.L75P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000322142
Start 105386367:105386379(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.138_150delCATCGGCTGTGAC
AA Mutation p.Ile47AlafsTer160(p.I47Afs*160)
Mutation Classification Frame_Shift_Del
Feature Type Transcript