Primary Site >> Stomach Cancer

Gene >> MSN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65729543:65729543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746950857
CDS Mutation c.298C>T
AA Mutation p.Arg100Cys(p.R100C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65737209:65737209(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1122A>C
AA Mutation p.Glu374Asp(p.E374D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65735348:65735348(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.877C>T
AA Mutation p.Arg293Cys(p.R293C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65716827:65716827(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759664613
CDS Mutation c.22C>T
AA Mutation p.Arg8Cys(p.R8C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65739180:65739180(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1555C>A
AA Mutation p.Gln519Lys(p.Q519K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65737195:65737195(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761864712
CDS Mutation c.1108C>T
AA Mutation p.Arg370Cys(p.R370C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65729606:65729606(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.361A>G
AA Mutation p.Thr121Ala(p.T121A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65716889:65716889(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.84G>C
AA Mutation p.Gln28His(p.Q28H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65727877:65727877(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.160G>A
AA Mutation p.Gly54Ser(p.G54S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360270
Start 65739837:65739837(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1678C>T
AA Mutation p.Arg560Cys(p.R560C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000360270
Start 65729515:65729515(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.270C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000360270
Start 65731967:65731967(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.681C>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000360270
Start 65733269:65733269(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.789delA
AA Mutation p.Ala264ProfsTer42(p.A264Pfs*42)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence splice_donor_variant
Transcription ID ENST00000360270
Start 65667855:65667855(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12+2T>C
Mutation Classification Splice_Site
Feature Type Transcript