Primary Site >> Stomach Cancer

Gene >> INSC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379554
Start 15200857:15200857(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373439305
CDS Mutation c.868C>T
AA Mutation p.Arg290Trp(p.R290W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379554
Start 15175949:15175949(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768595761
CDS Mutation c.406C>T
AA Mutation p.Arg136Cys(p.R136C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379554
Start 15225766:15225766(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375266524
CDS Mutation c.1249C>T
AA Mutation p.Arg417Cys(p.R417C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379554
Start 15235630:15235630(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1340T>C
AA Mutation p.Val447Ala(p.V447A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379554
Start 15149221:15149221(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.188C>A
AA Mutation p.Pro63Gln(p.P63Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000379554
Start 15239027:15239027(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771388775
CDS Mutation c.1487G>A
AA Mutation p.Arg496His(p.R496H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000379554
Start 15240516:15240516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1604C>T
AA Mutation p.Ala535Val(p.A535V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000379554
Start 15190807:15190807(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.827T>C
AA Mutation p.Ile276Thr(p.I276T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000379554
Start 15112479:15112479(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.14delC
AA Mutation p.Pro5LeufsTer44(p.P5Lfs*44)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence splice_donor_variant
Transcription ID ENST00000379554
Start 15225830:15225830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1311+2T>C
Mutation Classification Splice_Site
Feature Type Transcript