Primary Site >> Stomach Cancer

Gene >> MAP1B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72196857:72196857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3502T>A
AA Mutation p.Ser1168Thr(p.S1168T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72199993:72199993(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754794035
CDS Mutation c.6638G>A
AA Mutation p.Arg2213His(p.R2213H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72196810:72196810(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749214681
CDS Mutation c.3455C>T
AA Mutation p.Thr1152Met(p.T1152M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72196803:72196803(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3448G>A
AA Mutation p.Glu1150Lys(p.E1150K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72199992:72199992(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs573728562
CDS Mutation c.6637C>T
AA Mutation p.Arg2213Cys(p.R2213C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72115767:72115767(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.254G>T
AA Mutation p.Arg85Leu(p.R85L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72200161:72200161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6806C>A
AA Mutation p.Ala2269Glu(p.A2269E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72195783:72195783(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2428G>A
AA Mutation p.Ala810Thr(p.A810T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72197179:72197179(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372421201
CDS Mutation c.3824G>A
AA Mutation p.Arg1275His(p.R1275H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72195715:72195715(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2360A>C
AA Mutation p.Lys787Thr(p.K787T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72197745:72197745(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4390G>T
AA Mutation p.Asp1464Tyr(p.D1464Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72198741:72198741(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775654536
CDS Mutation c.5386T>C
AA Mutation p.Tyr1796His(p.Y1796H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72199269:72199269(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5914T>C
AA Mutation p.Tyr1972His(p.Y1972H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72194833:72194833(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140205740
CDS Mutation c.1478G>A
AA Mutation p.Ser493Asn(p.S493N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72198327:72198327(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4972C>A
AA Mutation p.Leu1658Ile(p.L1658I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72199197:72199197(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151255965
CDS Mutation c.5842C>T
AA Mutation p.Arg1948Trp(p.R1948W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72203746:72203746(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144647263
CDS Mutation c.7196G>A
AA Mutation p.Arg2399Gln(p.R2399Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72198418:72198418(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5063A>C
AA Mutation p.Asp1688Ala(p.D1688A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72197421:72197421(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4066C>T
AA Mutation p.Pro1356Ser(p.P1356S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72199965:72199965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6610C>T
AA Mutation p.Pro2204Ser(p.P2204S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72197920:72197920(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4565C>T
AA Mutation p.Ser1522Phe(p.S1522F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72196980:72196980(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3625C>T
AA Mutation p.Pro1209Ser(p.P1209S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000296755
Start 72195911:72195911(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2556G>T
AA Mutation p.Lys852Asn(p.K852N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72195131:72195131(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1776G>A
Mutation Classification Silent
Feature Type Transcript
ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72196901:72196901(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148313643
CDS Mutation c.3546G>A
Mutation Classification Silent
Feature Type Transcript
ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72194213:72194213(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777817448
CDS Mutation c.858C>T
Mutation Classification Silent
Feature Type Transcript
ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72199901:72199901(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs77733766
CDS Mutation c.6546C>T
Mutation Classification Silent
Feature Type Transcript
ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72195266:72195266(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140902387
CDS Mutation c.1911G>A
Mutation Classification Silent
Feature Type Transcript
ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72198869:72198869(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766462360
CDS Mutation c.5514C>T
Mutation Classification Silent
Feature Type Transcript
ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72196250:72196250(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs193173542
CDS Mutation c.2895C>T
Mutation Classification Silent
Feature Type Transcript
ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72196118:72196118(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs183520146
CDS Mutation c.2763C>T
Mutation Classification Silent
Feature Type Transcript
ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72197126:72197126(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757277389
CDS Mutation c.3771G>A
Mutation Classification Silent
Feature Type Transcript
ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72198320:72198320(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4965G>A
Mutation Classification Silent
Feature Type Transcript
ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72199532:72199532(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567310466
CDS Mutation c.6177C>T
Mutation Classification Silent
Feature Type Transcript
ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72195954:72195954(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2599C>T
Mutation Classification Silent
Feature Type Transcript
ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72194126:72194126(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.771C>T
Mutation Classification Silent
Feature Type Transcript
ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72194798:72194798(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533759374
CDS Mutation c.1443G>A
Mutation Classification Silent
Feature Type Transcript
ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000296755
Start 72199955:72199955(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6600A>G
Mutation Classification Silent
Feature Type Transcript
ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000296755
Start 72195396:72195396(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2046delA
AA Mutation p.Glu683LysfsTer39(p.E683Kfs*39)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 40
Mutation Consequence frameshift_variant
Transcription ID ENST00000296755
Start 72196465:72196465(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3115delA
AA Mutation p.Met1039TrpfsTer7(p.M1039Wfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000296755
Start 72200245:72200245(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.6893delA
AA Mutation p.Lys2298ArgfsTer90(p.K2298Rfs*90)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 42
Mutation Consequence frameshift_variant
Transcription ID ENST00000296755
Start 72195602:72195602(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2253delA
AA Mutation p.Lys751AsnfsTer5(p.K751Nfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 43
Mutation Consequence stop_gained
Transcription ID ENST00000296755
Start 72199380:72199380(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6025G>T
AA Mutation p.Glu2009Ter(p.E2009*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000296755
Start 72197163:72197164(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3814dupC
AA Mutation p.Leu1272ProfsTer3(p.L1272Pfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000296755
Start 72200090:72200091(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.6740dupA
AA Mutation p.Pro2248AlafsTer15(p.P2248Afs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000296755
Start 72195601:72195602(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2253dupA
AA Mutation p.Pro752ThrfsTer35(p.P752Tfs*35)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript