Primary Site >> Stomach Cancer

Gene >> CDH17

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000027335
Start 94130690:94130690(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2334C>A
AA Mutation p.His778Gln(p.H778Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000027335
Start 94176570:94176570(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.395A>G
AA Mutation p.Glu132Gly(p.E132G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000027335
Start 94162130:94162130(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs181733586
CDS Mutation c.1315G>A
AA Mutation p.Val439Ile(p.V439I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000027335
Start 94151881:94151881(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1783G>T
AA Mutation p.Gly595Cys(p.G595C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000027335
Start 94170519:94170519(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.944A>C
AA Mutation p.Glu315Ala(p.E315A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000027335
Start 94176572:94176572(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773708635
CDS Mutation c.393C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000027335
Start 94152002:94152002(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149027046
CDS Mutation c.1662G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000027335
Start 94146079:94146079(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148714244
CDS Mutation c.2016G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000027335
Start 94165900:94165900(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1143T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000027335
Start 94130933:94130933(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2227T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000027335
Start 94170538:94170538(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.925delT
AA Mutation p.Tyr309MetfsTer20(p.Y309Mfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000027335
Start 94174129:94174129(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.556delA
AA Mutation p.Thr186ArgfsTer14(p.T186Rfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000027335
Start 94174132:94174132(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.553A>T
AA Mutation p.Lys185Ter(p.K185*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000027335
Start 94170520:94170520(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.943G>T
AA Mutation p.Glu315Ter(p.E315*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000027335
Start 94152113:94152113(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1552-1G>T
Mutation Classification Splice_Site
Feature Type Transcript