Primary Site >> Stomach Cancer

Gene >> SLC2A2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000314251
Start 171007213:171007213(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368626129
CDS Mutation c.547G>A
AA Mutation p.Ala183Thr(p.A183T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000314251
Start 171007177:171007177(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.583G>A
AA Mutation p.Ala195Thr(p.A195T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000314251
Start 171007233:171007233(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.527T>C
AA Mutation p.Ile176Thr(p.I176T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000314251
Start 171006054:171006054(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.664C>T
AA Mutation p.Leu222Phe(p.L222F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000314251
Start 170999097:170999097(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1138G>A
AA Mutation p.Ala380Thr(p.A380T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000314251
Start 171006060:171006060(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.658A>G
AA Mutation p.Ile220Val(p.I220V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000314251
Start 171010022:171010022(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.432T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000314251
Start 171014545:171014557(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.283_295delATGCTCTGGTCCC
AA Mutation p.Met95CysfsTer11(p.M95Cfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript