Primary Site >> Stomach Cancer

Gene >> MEX3B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82043696:82043696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1174G>A
AA Mutation p.Val392Ile(p.V392I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82043206:82043206(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1664C>T
AA Mutation p.Pro555Leu(p.P555L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82043963:82043963(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.907G>A
AA Mutation p.Gly303Ser(p.G303S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82044011:82044011(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.859G>A
AA Mutation p.Asp287Asn(p.D287N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82043800:82043800(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1070C>A
AA Mutation p.Pro357His(p.P357H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82044499:82044499(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773623161
CDS Mutation c.371G>A
AA Mutation p.Arg124Gln(p.R124Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82044127:82044127(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.743T>C
AA Mutation p.Val248Ala(p.V248A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82043173:82043173(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1697G>A
AA Mutation p.Arg566His(p.R566H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82043191:82043191(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143849049
CDS Mutation c.1679C>T
AA Mutation p.Ala560Val(p.A560V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82043807:82043807(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1063G>A
AA Mutation p.Gly355Ser(p.G355S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000329713
Start 82043185:82043185(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1685C>T
AA Mutation p.Thr562Ile(p.T562I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000329713
Start 82044596:82044596(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.274C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000329713
Start 82044093:82044093(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.777C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000329713
Start 82043730:82043730(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1140C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000329713
Start 82044222:82044222(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.648C>T
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000329713
Start 82043616:82043616(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1254G>A
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000329713
Start 82043373:82043373(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1497C>A
Mutation Classification Silent
Feature Type Transcript
ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000329713
Start 82044051:82044051(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.819G>A
Mutation Classification Silent
Feature Type Transcript
ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000329713
Start 82043646:82043646(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1224C>T
Mutation Classification Silent
Feature Type Transcript
ID 20
Mutation Consequence frameshift_variant
Transcription ID ENST00000329713
Start 82043799:82043799(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1071delC
AA Mutation p.Glu358SerfsTer169(p.E358Sfs*169)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000329713
Start 82043833:82043833(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1037delG
AA Mutation p.Gly346GlufsTer181(p.G346Efs*181)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000329713
Start 82044042:82044042(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.828delC
AA Mutation p.Gly277AlafsTer49(p.G277Afs*49)
Mutation Classification Frame_Shift_Del
Feature Type Transcript