Primary Site >> Stomach Cancer

Gene >> THEMIS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127812974:127812974(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1667G>A
AA Mutation p.Arg556His(p.R556H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127813454:127813454(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1187C>T
AA Mutation p.Thr396Met(p.T396M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127829739:127829739(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759891900
CDS Mutation c.446T>C
AA Mutation p.Met149Thr(p.M149T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127855108:127855108(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.172A>G
AA Mutation p.Lys58Glu(p.K58E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127813691:127813691(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.950G>A
AA Mutation p.Arg317Lys(p.R317K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127719753:127719753(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1829G>T
AA Mutation p.Gly610Val(p.G610V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127719717:127719717(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1865G>T
AA Mutation p.Arg622Met(p.R622M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127813721:127813721(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779555672
CDS Mutation c.920T>C
AA Mutation p.Ile307Thr(p.I307T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127719708:127719708(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745362791
CDS Mutation c.1874G>A
AA Mutation p.Arg625His(p.R625H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000368248
Start 127813423:127813423(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1218delA
AA Mutation p.Val407TrpfsTer2(p.V407Wfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000368248
Start 127829671:127829671(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.514G>T
AA Mutation p.Glu172Ter(p.E172*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript