Primary Site >> Stomach Cancer

Gene >> SMC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000286398
Start 104127461:104127461(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2771C>A
AA Mutation p.Ala924Asp(p.A924D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000286398
Start 104127407:104127407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2717C>T
AA Mutation p.Ser906Phe(p.S906F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000286398
Start 104114009:104114009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1460G>A
AA Mutation p.Arg487His(p.R487H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000286398
Start 104138042:104138042(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3294A>G
AA Mutation p.Ile1098Met(p.I1098M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000286398
Start 104113992:104113992(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1443G>C
AA Mutation p.Lys481Asn(p.K481N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000286398
Start 104123148:104123148(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2173G>A
AA Mutation p.Glu725Lys(p.E725K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000286398
Start 104102188:104102188(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.865G>C
AA Mutation p.Asp289His(p.D289H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000286398
Start 104113338:104113338(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1277C>T
AA Mutation p.Ala426Val(p.A426V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000286398
Start 104111754:104111754(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs184176278
CDS Mutation c.1194T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000286398
Start 104127323:104127323(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2637delA
AA Mutation p.Glu880ArgfsTer2(p.E880Rfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000286398
Start 104123220:104123220(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2251delA
AA Mutation p.Thr751ProfsTer9(p.T751Pfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000286398
Start 104100169:104100169(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.563delA
AA Mutation p.Lys188ArgfsTer5(p.K188Rfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000286398
Start 104102557:104102557(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1010delA
AA Mutation p.Asn337IlefsTer9(p.N337Ifs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000286398
Start 104100141:104100141(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.535delA
AA Mutation p.Ile179Ter(p.I179*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000286398
Start 104120159:104120159(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2132delA
AA Mutation p.Lys711SerfsTer5(p.K711Sfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained;protein_altering_variant
Transcription ID ENST00000286398
Start 104129733:104129734(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2879_2880insATACTTTTGAAT
AA Mutation p.Asn960delinsLysTyrPheTerIle(p.N960delinsKYF*I)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000286398
Start 104100140:104100141(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.535dupA
AA Mutation p.Ile179AsnfsTer13(p.I179Nfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000286398
Start 104116224:104116225(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1702dupG
AA Mutation p.Glu568GlyfsTer13(p.E568Gfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript