Primary Site >> Stomach Cancer

Gene >> TNRC6A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791737:24791737(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749539505
CDS Mutation c.3095G>A
AA Mutation p.Arg1032His(p.R1032H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24805086:24805086(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4057C>G
AA Mutation p.Gln1353Glu(p.Q1353E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24816861:24816861(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4877C>A
AA Mutation p.Pro1626His(p.P1626H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791708:24791708(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3066G>T
AA Mutation p.Trp1022Cys(p.W1022C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24804267:24804267(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767157053
CDS Mutation c.3785G>A
AA Mutation p.Arg1262Gln(p.R1262Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24806231:24806231(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201497215
CDS Mutation c.4277C>T
AA Mutation p.Ala1426Val(p.A1426V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24790200:24790200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1558A>G
AA Mutation p.Thr520Ala(p.T520A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24794708:24794708(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3517A>G
AA Mutation p.Met1173Val(p.M1173V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24777185:24777185(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.416G>T
AA Mutation p.Arg139Leu(p.R139L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24790873:24790873(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753463751
CDS Mutation c.2231G>A
AA Mutation p.Arg744Gln(p.R744Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24806638:24806638(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4394T>C
AA Mutation p.Leu1465Ser(p.L1465S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791326:24791326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2684C>A
AA Mutation p.Ser895Tyr(p.S895Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791718:24791718(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374666136
CDS Mutation c.3076G>A
AA Mutation p.Val1026Ile(p.V1026I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24806658:24806658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4414C>T
AA Mutation p.Pro1472Ser(p.P1472S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791626:24791626(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2984T>C
AA Mutation p.Ile995Thr(p.I995T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24820151:24820151(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5093A>T
AA Mutation p.Asp1698Val(p.D1698V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24789714:24789714(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1072C>T
AA Mutation p.Pro358Ser(p.P358S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24823724:24823724(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770476613
CDS Mutation c.5806G>A
AA Mutation p.Asp1936Asn(p.D1936N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24809381:24809381(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4572T>A
AA Mutation p.Asp1524Glu(p.D1524E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24790071:24790071(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1429A>G
AA Mutation p.Ser477Gly(p.S477G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791298:24791298(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767104641
CDS Mutation c.2656G>A
AA Mutation p.Gly886Ser(p.G886S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24804848:24804848(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3981A>T
AA Mutation p.Arg1327Ser(p.R1327S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791631:24791631(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766143258
CDS Mutation c.2989C>T
AA Mutation p.Arg997Cys(p.R997C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24777119:24777119(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.350C>A
AA Mutation p.Pro117Gln(p.P117Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24794601:24794601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3410G>T
AA Mutation p.Arg1137Leu(p.R1137L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24794704:24794704(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3513G>T
AA Mutation p.Lys1171Asn(p.K1171N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24806748:24806748(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4504C>T
AA Mutation p.Pro1502Ser(p.P1502S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000395799
Start 24823543:24823543(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5625C>T
Mutation Classification Silent
Feature Type Transcript
ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000395799
Start 24791462:24791462(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2820A>T
Mutation Classification Silent
Feature Type Transcript
ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000395799
Start 24804304:24804304(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3822T>C
Mutation Classification Silent
Feature Type Transcript
ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000395799
Start 24793534:24793534(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3237A>G
Mutation Classification Silent
Feature Type Transcript
ID 32
Mutation Consequence frameshift_variant
Transcription ID ENST00000395799
Start 24795919:24795919(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3547delA
AA Mutation p.Arg1183GlyfsTer7(p.R1183Gfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000395799
Start 24791045:24791045(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2409delG
AA Mutation p.Trp804GlyfsTer99(p.W804Gfs*99)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000395799
Start 24823709:24823709(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5795delC
AA Mutation p.Pro1932GlnfsTer82(p.P1932Qfs*82)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000395799
Start 24823577:24823578(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5660_5661delGT
AA Mutation p.Cys1887PhefsTer22(p.C1887Ffs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 36
Mutation Consequence stop_gained
Transcription ID ENST00000395799
Start 24820332:24820332(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5274G>A
AA Mutation p.Trp1758Ter(p.W1758*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 37
Mutation Consequence inframe_deletion
Transcription ID ENST00000395799
Start 24777055:24777060(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.294_299delGCAGCA
AA Mutation p.Gln102_Gln103del(p.Q102_Q103del)
Mutation Classification In_Frame_Del
Feature Type Transcript