Primary Site >> Stomach Cancer

Gene >> ATR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142457619:142457619(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7640G>A
AA Mutation p.Arg2547Gln(p.R2547Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142497163:142497163(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5588G>A
AA Mutation p.Ser1863Asn(p.S1863N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142469500:142469500(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6389C>G
AA Mutation p.Thr2130Arg(p.T2130R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000350721
Start 142559439:142559439(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746970647
CDS Mutation c.1544G>A
AA Mutation p.Arg515His(p.R515H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142468014:142468014(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6607C>A
AA Mutation p.His2203Asn(p.H2203N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142512434:142512434(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756354361
CDS Mutation c.4678G>A
AA Mutation p.Asp1560Asn(p.D1560N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142459231:142459231(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7345T>C
AA Mutation p.Ser2449Pro(p.S2449P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142467960:142467960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6661A>G
AA Mutation p.Lys2221Glu(p.K2221E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142512274:142512274(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4838A>C
AA Mutation p.Lys1613Thr(p.K1613T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142524171:142524171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3974G>A
AA Mutation p.Ser1325Asn(p.S1325N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142566217:142566217(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.196G>C
AA Mutation p.Val66Leu(p.V66L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142556117:142556117(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2101G>A
AA Mutation p.Asp701Asn(p.D701N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142459031:142459031(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7430A>G
AA Mutation p.His2477Arg(p.H2477R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142549499:142549499(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367641692
CDS Mutation c.3151C>T
AA Mutation p.Arg1051Cys(p.R1051C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142449580:142449580(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7784T>G
AA Mutation p.Ile2595Ser(p.I2595S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142541010:142541010(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3475A>T
AA Mutation p.Met1159Leu(p.M1159L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142515428:142515428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4470G>T
AA Mutation p.Trp1490Cys(p.W1490C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000350721
Start 142547837:142547837(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146504354
CDS Mutation c.3245G>A
AA Mutation p.Arg1082His(p.R1082H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000350721
Start 142498677:142498677(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5478G>A
Mutation Classification Silent
Feature Type Transcript
ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000350721
Start 142556550:142556550(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1911G>A
Mutation Classification Silent
Feature Type Transcript
ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000350721
Start 142524149:142524149(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3996C>A
Mutation Classification Silent
Feature Type Transcript
ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000350721
Start 142499715:142499715(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745745176
CDS Mutation c.5292C>T
Mutation Classification Silent
Feature Type Transcript
ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000350721
Start 142553395:142553395(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150512706
CDS Mutation c.2637C>T
Mutation Classification Silent
Feature Type Transcript
ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000350721
Start 142549560:142549560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3090A>C
Mutation Classification Silent
Feature Type Transcript
ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000350721
Start 142547857:142547857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3225G>A
Mutation Classification Silent
Feature Type Transcript
ID 26
Mutation Consequence frameshift_variant
Transcription ID ENST00000350721
Start 142542713:142542713(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3402delT
AA Mutation p.Phe1134LeufsTer6(p.F1134Lfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 27
Mutation Consequence frameshift_variant
Transcription ID ENST00000350721
Start 142498715:142498715(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5440delA
AA Mutation p.Arg1814GlufsTer10(p.R1814Efs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 28
Mutation Consequence frameshift_variant
Transcription ID ENST00000350721
Start 142468003:142468003(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.6618delA
AA Mutation p.Lys2206AsnfsTer3(p.K2206Nfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 29
Mutation Consequence frameshift_variant
Transcription ID ENST00000350721
Start 142559357:142559357(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1626delA
AA Mutation p.Val543CysfsTer9(p.V543Cfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 30
Mutation Consequence frameshift_variant
Transcription ID ENST00000350721
Start 142549538:142549538(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3112delT
AA Mutation p.Ser1038LeufsTer12(p.S1038Lfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000350721
Start 142469473:142469473(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.6416delT
AA Mutation p.Leu2139Ter(p.L2139*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000350721
Start 142556558:142556558(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1903C>T
AA Mutation p.Arg635Ter(p.R635*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000350721
Start 142524078:142524079(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.4066dupG
AA Mutation p.Glu1356GlyfsTer20(p.E1356Gfs*20)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 34
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000350721
Start 142563110:142563110(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.293-1G>T
Mutation Classification Splice_Site
Feature Type Transcript