Primary Site >> Stomach Cancer

Gene >> DVL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000378888
Start 1338560:1338560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1301G>A
AA Mutation p.Arg434His(p.R434H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000378888
Start 1340129:1340129(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375062198
CDS Mutation c.818G>A
AA Mutation p.Arg273His(p.R273H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000378888
Start 1338371:1338371(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1405A>G
AA Mutation p.Lys469Glu(p.K469E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000378888
Start 1339757:1339757(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767570616
CDS Mutation c.965G>A
AA Mutation p.Arg322Gln(p.R322Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000378888
Start 1340138:1340138(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.809G>T
AA Mutation p.Ser270Ile(p.S270I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000378888
Start 1342437:1342437(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767846983
CDS Mutation c.288G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000378888
Start 1339771:1339771(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779553612
CDS Mutation c.951C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000378888
Start 1338054:1338054(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs797044839
CDS Mutation c.1637delC
AA Mutation p.Pro546HisfsTer128(p.P546Hfs*128)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000378888
Start 1341748:1341748(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.524delC
AA Mutation p.Pro175GlnfsTer66(p.P175Qfs*66)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000378888
Start 1338098:1338098(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1593delC
AA Mutation p.Trp532GlyfsTer142(p.W532Gfs*142)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000378888
Start 1338573:1338573(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1288G>T
AA Mutation p.Glu430Ter(p.E430*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000378888
Start 1338053:1338054(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1637dupC
AA Mutation p.Pro547ThrfsTer13(p.P547Tfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript