Primary Site >> Stomach Cancer

Gene >> TRIP6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000200457
Start 100871622:100871622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1079C>A
AA Mutation p.Pro360His(p.P360H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000200457
Start 100870636:100870636(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750780514
CDS Mutation c.892C>T
AA Mutation p.Arg298Cys(p.R298C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000200457
Start 100871616:100871616(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1073A>G
AA Mutation p.Tyr358Cys(p.Y358C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000200457
Start 100871651:100871651(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774097015
CDS Mutation c.1108C>T
AA Mutation p.Arg370Cys(p.R370C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000200457
Start 100872652:100872652(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201241149
CDS Mutation c.1207G>A
AA Mutation p.Gly403Ser(p.G403S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000200457
Start 100871628:100871628(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1085G>C
AA Mutation p.Cys362Ser(p.C362S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000200457
Start 100870669:100870669(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.925A>G
AA Mutation p.Thr309Ala(p.T309A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000200457
Start 100872729:100872729(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1284C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000200457
Start 100870707:100870707(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.963C>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000200457
Start 100868124:100868124(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.260delG
AA Mutation p.Gly87AlafsTer11(p.G87Afs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript