Primary Site >> Stomach Cancer

Gene >> SLC7A11

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000280612
Start 138219359:138219359(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs186693425
CDS Mutation c.653C>T
AA Mutation p.Thr218Met(p.T218M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000280612
Start 138182331:138182331(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1082G>A
AA Mutation p.Arg361His(p.R361H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000280612
Start 138180749:138180749(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1158C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000280612
Start 138241839:138241839(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.231C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000280612
Start 138232301:138232301(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.486A>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000280612
Start 138232322:138232322(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.465delT
AA Mutation p.Phe155LeufsTer19(p.F155Lfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript