Primary Site >> Stomach Cancer

Gene >> FLCN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000285071
Start 17228015:17228015(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.123G>T
AA Mutation p.Gln41His(p.Q41H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000285071
Start 17219091:17219091(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.990C>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000285071
Start 17223949:17223949(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763617124
CDS Mutation c.591C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000285071
Start 17216414:17216414(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751013842
CDS Mutation c.1266G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000285071
Start 17226266:17226266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.306C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000285071
Start 17213784:17213784(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1611C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000285071
Start 17223994:17223994(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.546C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000285071
Start 17215188:17215188(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1429C>T
AA Mutation p.Arg477Ter(p.R477*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000285071
Start 17213816:17213816(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1579C>T
AA Mutation p.Arg527Ter(p.R527*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript