Primary Site >> Stomach Cancer

Gene >> RAPH1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000319170
Start 203489699:203489699(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.617A>T
AA Mutation p.Asn206Ile(p.N206I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000319170
Start 203440902:203440902(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2288C>A
AA Mutation p.Pro763His(p.P763H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000319170
Start 203441319:203441319(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1871C>A
AA Mutation p.Pro624His(p.P624H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000319170
Start 203441131:203441131(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2059C>T
AA Mutation p.Pro687Ser(p.P687S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000319170
Start 203444929:203444929(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1715T>G
AA Mutation p.Ile572Ser(p.I572S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000319170
Start 203489673:203489673(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772560358
CDS Mutation c.643G>C
AA Mutation p.Ala215Pro(p.A215P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000319170
Start 203489853:203489853(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145036827
CDS Mutation c.463G>A
AA Mutation p.Asp155Asn(p.D155N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000319170
Start 203489670:203489670(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.646G>T
AA Mutation p.Ala216Ser(p.A216S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000319170
Start 203489630:203489630(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs561862665
CDS Mutation c.686G>A
AA Mutation p.Arg229His(p.R229H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000319170
Start 203439562:203439562(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3628C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000319170
Start 203440658:203440658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2532G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000319170
Start 203489674:203489674(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760714383
CDS Mutation c.642C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000319170
Start 203454444:203454453(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1390_1399delACAGACTATT
AA Mutation p.Thr464ValfsTer4(p.T464Vfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000319170
Start 203441075:203441075(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2115delC
AA Mutation p.Asn706MetfsTer23(p.N706Mfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000319170
Start 203461369:203461369(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.850delA
AA Mutation p.Thr284GlnfsTer2(p.T284Qfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000319170
Start 203455478:203455478(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1261C>T
AA Mutation p.Arg421Ter(p.R421*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000319170
Start 203440114:203440115(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3075dupC
AA Mutation p.Lys1026GlnfsTer47(p.K1026Qfs*47)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000319170
Start 203441074:203441075(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2115dupC
AA Mutation p.Asn706GlnfsTer217(p.N706Qfs*217)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 19
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000319170
Start 203445011:203445011(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1634-1G>T
Mutation Classification Splice_Site
Feature Type Transcript