Primary Site >> Stomach Cancer

Gene >> SEMA4C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000305476
Start 96861096:96861096(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2032G>C
AA Mutation p.Val678Leu(p.V678L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000305476
Start 96860655:96860655(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146332513
CDS Mutation c.2473G>A
AA Mutation p.Asp825Asn(p.D825N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000305476
Start 96864329:96864329(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377346652
CDS Mutation c.1016G>A
AA Mutation p.Arg339Gln(p.R339Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000305476
Start 96860756:96860756(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2372G>A
AA Mutation p.Arg791His(p.R791H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000305476
Start 96864276:96864276(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371197229
CDS Mutation c.1069C>T
AA Mutation p.Arg357Cys(p.R357C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000305476
Start 96865261:96865261(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.577C>T
AA Mutation p.Arg193Cys(p.R193C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000305476
Start 96866343:96866343(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.198C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000305476
Start 96860852:96860852(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2276delC
AA Mutation p.Pro759LeufsTer36(p.P759Lfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000305476
Start 96861153:96861153(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1975delC
AA Mutation p.Leu659TrpfsTer87(p.L659Wfs*87)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000305476
Start 96864022:96864022(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1234delC
AA Mutation p.Leu412CysfsTer3(p.L412Cfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000305476
Start 96860857:96860857(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2271delG
AA Mutation p.Pro759LeufsTer36(p.P759Lfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript