Primary Site >> Stomach Cancer

Gene >> BIRC6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32443555:32443555(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4303A>G
AA Mutation p.Asn1435Asp(p.N1435D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32401479:32401479(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1274A>T
AA Mutation p.Glu425Val(p.E425V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32468544:32468544(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5888C>T
AA Mutation p.Ala1963Val(p.A1963V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32478798:32478798(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7232T>C
AA Mutation p.Met2411Thr(p.M2411T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32547990:32547990(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12951G>C
AA Mutation p.Glu4317Asp(p.E4317D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32482567:32482567(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144411884
CDS Mutation c.7681G>A
AA Mutation p.Val2561Ile(p.V2561I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32415555:32415555(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2264A>C
AA Mutation p.Glu755Ala(p.E755A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32490085:32490085(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8140A>C
AA Mutation p.Thr2714Pro(p.T2714P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32529743:32529743(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12013A>C
AA Mutation p.Thr4005Pro(p.T4005P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32543482:32543482(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12533G>T
AA Mutation p.Arg4178Ile(p.R4178I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32595073:32595073(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13541A>C
AA Mutation p.Lys4514Thr(p.K4514T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32467548:32467548(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5380G>A
AA Mutation p.Asp1794Asn(p.D1794N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32482436:32482436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776298375
CDS Mutation c.7550G>A
AA Mutation p.Ser2517Asn(p.S2517N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32515418:32515418(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759663407
CDS Mutation c.10997G>A
AA Mutation p.Arg3666His(p.R3666H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32469557:32469557(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6290C>T
AA Mutation p.Ser2097Phe(p.S2097F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32401243:32401243(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1115T>C
AA Mutation p.Leu372Pro(p.L372P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32599769:32599769(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13861T>A
AA Mutation p.Tyr4621Asn(p.Y4621N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32515688:32515688(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138598333
CDS Mutation c.11267G>A
AA Mutation p.Arg3756His(p.R3756H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32448835:32448835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4525G>A
AA Mutation p.Asp1509Asn(p.D1509N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32478660:32478660(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766592234
CDS Mutation c.7094C>T
AA Mutation p.Thr2365Met(p.T2365M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32503141:32503141(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367580642
CDS Mutation c.9404C>G
AA Mutation p.Ser3135Cys(p.S3135C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32597936:32597936(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773885941
CDS Mutation c.13798C>T
AA Mutation p.Arg4600Cys(p.R4600C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32603072:32603072(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.14059A>C
AA Mutation p.Ser4687Arg(p.S4687R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32463274:32463274(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4834G>A
AA Mutation p.Ala1612Thr(p.A1612T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32453868:32453868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4679T>C
AA Mutation p.Leu1560Pro(p.L1560P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32415012:32415012(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1721C>A
AA Mutation p.Thr574Lys(p.T574K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32525574:32525574(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11866G>A
AA Mutation p.Ala3956Thr(p.A3956T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32549341:32549341(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.13004G>C
AA Mutation p.Ser4335Thr(p.S4335T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32430936:32430936(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3094G>A
AA Mutation p.Glu1032Lys(p.E1032K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32445535:32445535(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4351T>C
AA Mutation p.Tyr1451His(p.Y1451H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32439565:32439565(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3689G>T
AA Mutation p.Arg1230Ile(p.R1230I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32479527:32479527(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7318G>A
AA Mutation p.Ala2440Thr(p.A2440T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32439556:32439556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3680T>C
AA Mutation p.Val1227Ala(p.V1227A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32453903:32453903(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4714T>C
AA Mutation p.Ser1572Pro(p.S1572P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32525509:32525509(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766431375
CDS Mutation c.11801G>A
AA Mutation p.Arg3934His(p.R3934H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000421745
Start 32531493:32531493(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12233G>A
AA Mutation p.Gly4078Asp(p.G4078D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32401223:32401223(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1095T>C
Mutation Classification Silent
Feature Type Transcript
ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32401238:32401238(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1110C>A
Mutation Classification Silent
Feature Type Transcript
ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32575271:32575271(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13260T>C
Mutation Classification Silent
Feature Type Transcript
ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32499652:32499652(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs550913772
CDS Mutation c.8574C>T
Mutation Classification Silent
Feature Type Transcript
ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32515716:32515716(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371274962
CDS Mutation c.11295G>A
Mutation Classification Silent
Feature Type Transcript
ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32543246:32543246(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12297T>C
Mutation Classification Silent
Feature Type Transcript
ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32478691:32478691(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7125G>A
Mutation Classification Silent
Feature Type Transcript
ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32416093:32416093(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2802T>C
Mutation Classification Silent
Feature Type Transcript
ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32415394:32415394(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142938281
CDS Mutation c.2103G>A
Mutation Classification Silent
Feature Type Transcript
ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000421745
Start 32433692:32433692(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3297T>C
Mutation Classification Silent
Feature Type Transcript
ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000421745
Start 32464770:32464770(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5207delC
AA Mutation p.Pro1736GlnfsTer17(p.P1736Qfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000421745
Start 32525524:32525524(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.11820delG
AA Mutation p.Arg3941GlyfsTer7(p.R3941Gfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000421745
Start 32465071:32465077(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5265_5271delTGGTTCT
AA Mutation p.Gly1756ValfsTer2(p.G1756Vfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 50
Mutation Consequence stop_gained
Transcription ID ENST00000421745
Start 32490044:32490044(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8099C>G
AA Mutation p.Ser2700Ter(p.S2700*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000421745
Start 32524962:32524962(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11698G>T
AA Mutation p.Glu3900Ter(p.E3900*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000421745
Start 32415763:32415763(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2472T>A
AA Mutation p.Tyr824Ter(p.Y824*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 53
Mutation Consequence stop_gained
Transcription ID ENST00000421745
Start 32599868:32599868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13960C>T
AA Mutation p.Arg4654Ter(p.R4654*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 54
Mutation Consequence frameshift_variant
Transcription ID ENST00000421745
Start 32448807:32448808(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4498dupA
AA Mutation p.Ser1500LysfsTer5(p.S1500Kfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 55
Mutation Consequence frameshift_variant
Transcription ID ENST00000421745
Start 32611461:32611462(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.14278dupT
AA Mutation p.Tyr4760LeufsTer6(p.Y4760Lfs*6)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 56
Mutation Consequence inframe_insertion
Transcription ID ENST00000421745
Start 32611553:32611554(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.14366_14367insATC
AA Mutation p.Thr4789_Met4790insSer(p.T4789_M4790insS)
Mutation Classification In_Frame_Ins
Feature Type Transcript