Primary Site >> Stomach Cancer

Gene >> MSH3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265081
Start 80768923:80768923(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200612739
CDS Mutation c.2173G>A
AA Mutation p.Glu725Lys(p.E725K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265081
Start 80813632:80813632(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763041578
CDS Mutation c.2704A>C
AA Mutation p.Lys902Gln(p.K902Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265081
Start 80679002:80679002(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143211109
CDS Mutation c.1249C>T
AA Mutation p.Arg417Trp(p.R417W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265081
Start 80787576:80787576(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2447A>G
AA Mutation p.Glu816Gly(p.E816G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265081
Start 80670206:80670206(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763873895
CDS Mutation c.689C>T
AA Mutation p.Thr230Met(p.T230M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265081
Start 80778788:80778788(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs542104580
CDS Mutation c.2387G>A
AA Mutation p.Arg796Gln(p.R796Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000265081
Start 80670187:80670187(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748207601
CDS Mutation c.670C>T
AA Mutation p.Arg224Trp(p.R224W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000265081
Start 80813614:80813614(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777054839
CDS Mutation c.2686G>A
AA Mutation p.Gly896Arg(p.G896R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000265081
Start 80768922:80768922(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs541680738
CDS Mutation c.2172C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000265081
Start 80675096:80675096(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs752887309
CDS Mutation c.1148delA
AA Mutation p.Lys383ArgfsTer32(p.K383Rfs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000265081
Start 80778822:80778822(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2421G>A
AA Mutation p.Trp807Ter(p.W807*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000265081
Start 80675095:80675096(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1148dupA
AA Mutation p.Asn385GlnfsTer19(p.N385Qfs*19)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000265081
Start 80854129:80854129(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2814-1G>A
Mutation Classification Splice_Site
Feature Type Transcript