Primary Site >> Stomach Cancer

Gene >> CDH1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68808560:68808560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.524T>C
AA Mutation p.Leu175Pro(p.L175P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68810251:68810251(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.742A>T
AA Mutation p.Ile248Phe(p.I248F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68810269:68810269(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.760G>T
AA Mutation p.Asp254Tyr(p.D254Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68811764:68811764(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.913C>A
AA Mutation p.Leu305Ile(p.L305I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68811714:68811714(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.863A>T
AA Mutation p.Asp288Val(p.D288V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68808730:68808730(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.569A>G
AA Mutation p.Tyr190Cys(p.Y190C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68829684:68829684(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2326C>A
AA Mutation p.Leu776Met(p.L776M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68828254:68828254(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776975632
CDS Mutation c.2245C>T
AA Mutation p.Arg749Trp(p.R749W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000261769
Start 68813495:68813495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1320G>T
AA Mutation p.Lys440Asn(p.K440N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68811746:68811746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.895G>T
AA Mutation p.Ala299Ser(p.A299S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68808512:68808512(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.476C>T
AA Mutation p.Pro159Leu(p.P159L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68801810:68801810(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368492235
CDS Mutation c.304G>A
AA Mutation p.Ala102Thr(p.A102T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68810279:68810279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.770A>G
AA Mutation p.Asp257Gly(p.D257G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68823533:68823533(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2071G>A
AA Mutation p.Ala691Thr(p.A691T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68813379:68813379(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1204G>C
AA Mutation p.Asp402His(p.D402H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68812147:68812147(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1021T>G
AA Mutation p.Tyr341Asp(p.Y341D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68811746:68811746(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.895G>A
AA Mutation p.Ala299Thr(p.A299T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68808724:68808724(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.563T>A
AA Mutation p.Val188Asp(p.V188D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68810278:68810278(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.769G>A
AA Mutation p.Asp257Asn(p.D257N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68823518:68823518(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2056T>C
AA Mutation p.Cys686Arg(p.C686R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68808796:68808796(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.635G>A
AA Mutation p.Gly212Glu(p.G212E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68811720:68811720(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.869A>G
AA Mutation p.Asp290Gly(p.D290G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68808825:68808825(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.664A>G
AA Mutation p.Arg222Gly(p.R222G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68815683:68815683(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1489G>A
AA Mutation p.Glu497Lys(p.E497K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000261769
Start 68811857:68811857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1006G>A
AA Mutation p.Glu336Lys(p.E336K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68819390:68819390(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1676G>A
AA Mutation p.Ser559Asn(p.S559N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68808491:68808491(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.455A>G
AA Mutation p.Gln152Arg(p.Q152R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68801876:68801876(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748086082
CDS Mutation c.370C>T
AA Mutation p.Arg124Cys(p.R124C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000261769
Start 68813374:68813374(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1199A>T
AA Mutation p.Asp400Val(p.D400V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000261769
Start 68828289:68828289(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768547540
CDS Mutation c.2280C>T
Mutation Classification Silent
Feature Type Transcript
ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000261769
Start 68828214:68828214(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138493551
CDS Mutation c.2205G>A
Mutation Classification Silent
Feature Type Transcript
ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000261769
Start 68801782:68801782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.276T>C
Mutation Classification Silent
Feature Type Transcript
ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000261769
Start 68810208:68810208(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs115494727
CDS Mutation c.699C>T
Mutation Classification Silent
Feature Type Transcript
ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000261769
Start 68808553:68808553(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.521delA
AA Mutation p.Asn174ThrfsTer41(p.N174Tfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000261769
Start 68801710:68801710(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.208delT
AA Mutation p.Ser70ProfsTer13(p.S70Pfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000261769
Start 68801877:68801878(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.377dupC
AA Mutation p.Pro127AlafsTer41(p.P127Afs*41)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 37
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000261769
Start 68808692:68808692(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.532-1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 38
Mutation Consequence splice_donor_variant;coding_sequence_variant
Transcription ID ENST00000261769
Start 68808848:68808849(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.687+1_687+2delGT
Mutation Classification Splice_Site
Feature Type Transcript
ID 39
Mutation Consequence splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000261769
Start 68813475:68813515(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1301_1320+21delGCATTTTGAAAACAGCAAAGGTTTGTATGGTACCTGGCAAG
Mutation Classification Splice_Site
Feature Type Transcript
ID 40
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000261769
Start 68812133:68812133(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1009-2A>G
Mutation Classification Splice_Site
Feature Type Transcript
ID 41
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000261769
Start 68810196:68810196(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.688-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
ID 42
Mutation Consequence splice_donor_variant
Transcription ID ENST00000261769
Start 68822226:68822226(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1936+1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 43
Mutation Consequence splice_donor_variant
Transcription ID ENST00000261769
Start 68813496:68813496(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1320+1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 44
Mutation Consequence splice_donor_variant;coding_sequence_variant
Transcription ID ENST00000261769
Start 68829794:68829798(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2437_2439+2delGAAGT
Mutation Classification Splice_Site
Feature Type Transcript
ID 45
Mutation Consequence splice_donor_variant
Transcription ID ENST00000261769
Start 68808849:68808849(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.687+1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 46
Mutation Consequence inframe_deletion
Transcription ID ENST00000261769
Start 68811798:68811800(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.948_950delGTT
AA Mutation p.Met316_Phe317delinsIle(p.M316_F317delinsI)
Mutation Classification In_Frame_Del
Feature Type Transcript