Primary Site >> Liver Cancer

Gene >> ROS1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368508
Start 117288607:117288607(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6929A>C
AA Mutation p.His2310Pro(p.H2310P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368508
Start 117288640:117288640(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6896C>G
AA Mutation p.Ser2299Cys(p.S2299C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000368508
Start 117397000:117397000(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.694C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000368508
Start 117365088:117365088(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3090A>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000368508
Start 117317167:117317167(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6111T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000368508
Start 117425550:117425550(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.107C>A
AA Mutation p.Ser36Ter(p.S36*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000368508
Start 117387995:117387995(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1799T>G
AA Mutation p.Leu600Ter(p.L600*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript