Primary Site >> Stomach Cancer

Gene >> ANAPC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000341068
Start 111821297:111821297(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3148A>G
AA Mutation p.Asn1050Asp(p.N1050D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000341068
Start 111788286:111788286(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760585060
CDS Mutation c.4747G>A
AA Mutation p.Ala1583Thr(p.A1583T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000341068
Start 111843452:111843452(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2000T>C
AA Mutation p.Met667Thr(p.M667T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000341068
Start 111825809:111825809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2672A>C
AA Mutation p.Glu891Ala(p.E891A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000341068
Start 111880624:111880624(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.202G>A
AA Mutation p.Glu68Lys(p.E68K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000341068
Start 111862452:111862452(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368906308
CDS Mutation c.1199C>T
AA Mutation p.Thr400Met(p.T400M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000341068
Start 111785394:111785394(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751341287
CDS Mutation c.4883C>T
AA Mutation p.Thr1628Met(p.T1628M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000341068
Start 111863790:111863790(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.937T>C
AA Mutation p.Ser313Pro(p.S313P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000341068
Start 111850900:111850900(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1526T>C
AA Mutation p.Val509Ala(p.V509A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000341068
Start 111863734:111863734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.993A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000341068
Start 111821313:111821313(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3132G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000341068
Start 111794880:111794880(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4311T>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000341068
Start 111863858:111863858(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.869delG
AA Mutation p.Gly290GlufsTer26(p.G290Efs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000341068
Start 111821333:111821333(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3112C>T
AA Mutation p.Arg1038Ter(p.R1038*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000341068
Start 111825161:111825162(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2710dupC
AA Mutation p.Gln904ProfsTer13(p.Q904Pfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript