Primary Site >> Stomach Cancer

Gene >> BCOR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40074085:40074085(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200031455
CDS Mutation c.1261G>A
AA Mutation p.Gly421Ser(p.G421S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40072597:40072597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2749A>G
AA Mutation p.Thr917Ala(p.T917A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40073898:40073898(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs587778096
CDS Mutation c.1448C>T
AA Mutation p.Pro483Leu(p.P483L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000378444
Start 40055368:40055368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4741G>T
AA Mutation p.Asp1581Tyr(p.D1581Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40073742:40073742(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1604C>T
AA Mutation p.Ala535Val(p.A535V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40063801:40063801(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3654G>T
AA Mutation p.Trp1218Cys(p.W1218C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40073749:40073749(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1597G>A
AA Mutation p.Asp533Asn(p.D533N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40074667:40074667(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.679T>C
AA Mutation p.Tyr227His(p.Y227H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40075159:40075159(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.187A>G
AA Mutation p.Arg63Gly(p.R63G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40052306:40052306(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5071A>G
AA Mutation p.Thr1691Ala(p.T1691A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40062837:40062837(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4082G>C
AA Mutation p.Arg1361Thr(p.R1361T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000378444
Start 40073452:40073452(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762605753
CDS Mutation c.1894G>A
AA Mutation p.Gly632Ser(p.G632S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000378444
Start 40074569:40074569(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs576246224
CDS Mutation c.777G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000378444
Start 40072430:40072430(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370067698
CDS Mutation c.2916C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000378444
Start 40057265:40057265(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754796420
CDS Mutation c.4485C>T
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000378444
Start 40073315:40073315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2031A>G
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000378444
Start 40074083:40074083(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1263C>T
Mutation Classification Silent
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40054000:40054000(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs797044647
CDS Mutation c.4862delC
AA Mutation p.Pro1621GlnfsTer53(p.P1621Qfs*53)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 19
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40073541:40073541(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1805delC
AA Mutation p.Pro602ArgfsTer67(p.P602Rfs*67)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 20
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40063834:40063834(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3621delA
AA Mutation p.Lys1207AsnfsTer31(p.K1207Nfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40057227:40057227(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4523delG
AA Mutation p.Gly1508AlafsTer60(p.G1508Afs*60)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40072832:40072832(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2514delC
AA Mutation p.Lys839SerfsTer17(p.K839Sfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 23
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40074147:40074147(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1199delG
AA Mutation p.Gly400AlafsTer42(p.G400Afs*42)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 24
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40074874:40074874(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.472delA
AA Mutation p.Ser158ValfsTer3(p.S158Vfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 25
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40077911:40077911(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.19delC
AA Mutation p.Leu7CysfsTer9(p.L7Cfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 26
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40054012:40054012(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4850delT
AA Mutation p.Leu1617Ter(p.L1617*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 27
Mutation Consequence stop_gained
Transcription ID ENST00000378444
Start 40064351:40064351(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3487C>T
AA Mutation p.Arg1163Ter(p.R1163*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence stop_gained
Transcription ID ENST00000378444
Start 40073416:40073416(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1930G>T
AA Mutation p.Glu644Ter(p.E644*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence stop_gained
Transcription ID ENST00000378444
Start 40072510:40072510(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2836G>T
AA Mutation p.Glu946Ter(p.E946*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence stop_gained
Transcription ID ENST00000378444
Start 40072918:40072918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2428C>T
AA Mutation p.Arg810Ter(p.R810*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence stop_gained
Transcription ID ENST00000378444
Start 40073734:40073734(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1612C>T
AA Mutation p.Gln538Ter(p.Q538*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000378444
Start 40072414:40072414(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2932A>T
AA Mutation p.Lys978Ter(p.K978*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence stop_gained
Transcription ID ENST00000378444
Start 40057210:40057210(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4540C>T
AA Mutation p.Arg1514Ter(p.R1514*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 34
Mutation Consequence stop_gained
Transcription ID ENST00000378444
Start 40052216:40052216(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5161A>T
AA Mutation p.Lys1721Ter(p.K1721*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence stop_gained
Transcription ID ENST00000378444
Start 40063806:40063806(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3649C>T
AA Mutation p.Arg1217Ter(p.R1217*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40072556:40072557(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2789dupC
AA Mutation p.Pro931ThrfsTer15(p.P931Tfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 37
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40072534:40072535(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2811dupC
AA Mutation p.Thr938HisfsTer8(p.T938Hfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 38
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40063833:40063834(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3621dupA
AA Mutation p.Gln1208ThrfsTer8(p.Q1208Tfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000378444
Start 40055446:40055447(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4662dupT
AA Mutation p.Asp1555Ter(p.D1555*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 40
Mutation Consequence splice_donor_variant
Transcription ID ENST00000378444
Start 40062744:40062744(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4173+2T>C
Mutation Classification Splice_Site
Feature Type Transcript