Primary Site >> Stomach Cancer

Gene >> DEPDC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000456315
Start 68482332:68482332(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1476A>C
AA Mutation p.Gln492His(p.Q492H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000456315
Start 68482790:68482790(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1018A>G
AA Mutation p.Lys340Glu(p.K340E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000456315
Start 68481455:68481455(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1920G>T
AA Mutation p.Met640Ile(p.M640I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000456315
Start 68482787:68482787(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1021T>A
AA Mutation p.Ser341Thr(p.S341T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000456315
Start 68484006:68484006(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.854A>T
AA Mutation p.Asp285Val(p.D285V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000456315
Start 68479150:68479150(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2106G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000456315
Start 68482113:68482113(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776110439
CDS Mutation c.1695C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000456315
Start 68494627:68494627(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.117delA
AA Mutation p.Lys39AsnfsTer19(p.K39Nfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000456315
Start 68482535:68482535(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1273G>T
AA Mutation p.Gly425Ter(p.G425*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence start_lost;inframe_deletion
Transcription ID ENST00000456315
Start 68496993:68496998(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2_7delTGGAGA
AA Mutation p.MetGlu1_?2(p.ME1_?2)
Mutation Classification Translation_Start_Site
Feature Type Transcript