Primary Site >> Stomach Cancer

Gene >> RHOA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49368536:49368536(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.169T>G
AA Mutation p.Leu57Val(p.L57V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49375465:49375465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.125A>C
AA Mutation p.Tyr42Ser(p.Y42S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49368520:49368520(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.185G>A
AA Mutation p.Gly62Glu(p.G62E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49375465:49375465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.125A>G
AA Mutation p.Tyr42Cys(p.Y42C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49375474:49375474(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.116T>G
AA Mutation p.Phe39Cys(p.F39C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49368523:49368523(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.182C>A
AA Mutation p.Ala61Asp(p.A61D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49375489:49375489(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.101A>G
AA Mutation p.Tyr34Cys(p.Y34C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49375576:49375576(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs11552758
CDS Mutation c.14G>A
AA Mutation p.Arg5Gln(p.R5Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49368526:49368526(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.179C>A
AA Mutation p.Thr60Lys(p.T60K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49375540:49375540(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs11552761
CDS Mutation c.50G>A
AA Mutation p.Gly17Glu(p.G17E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49375472:49375472(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.118G>A
AA Mutation p.Glu40Lys(p.E40K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49368530:49368530(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.175G>T
AA Mutation p.Asp59Tyr(p.D59Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49375513:49375513(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.77G>T
AA Mutation p.Ser26Ile(p.S26I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49375577:49375577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13C>T
AA Mutation p.Arg5Trp(p.R5W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000418115
Start 49368521:49368521(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.184G>A
AA Mutation p.Gly62Arg(p.G62R)
Mutation Classification Missense_Mutation
Feature Type Transcript