Primary Site >> Stomach Cancer

Gene >> FHL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000345434
Start 136206503:136206503(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.71G>A
AA Mutation p.Gly24Asp(p.G24D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000345434
Start 136208564:136208564(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.611A>C
AA Mutation p.Glu204Ala(p.E204A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000345434
Start 136209281:136209281(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749585308
CDS Mutation c.727A>G
AA Mutation p.Lys243Glu(p.K243E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000345434
Start 136208502:136208502(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.549C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000345434
Start 136207844:136207844(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.384C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000345434
Start 136207129:136207130(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.272dupA
AA Mutation p.Cys92ValfsTer39(p.C92Vfs*39)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript