Primary Site >> Stomach Cancer

Gene >> SLC7A1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000380752
Start 29517597:29517597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1486G>A
AA Mutation p.Val496Met(p.V496M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000380752
Start 29523417:29523417(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763171472
CDS Mutation c.898G>A
AA Mutation p.Ala300Thr(p.A300T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000380752
Start 29523300:29523300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1015G>A
AA Mutation p.Val339Met(p.V339M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000380752
Start 29523389:29523389(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746536517
CDS Mutation c.926C>T
AA Mutation p.Thr309Met(p.T309M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000380752
Start 29523401:29523401(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.914C>T
AA Mutation p.Ser305Leu(p.S305L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000380752
Start 29535867:29535867(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.322C>T
AA Mutation p.Leu108Phe(p.L108F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000380752
Start 29530582:29530582(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751896544
CDS Mutation c.660G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000380752
Start 29522345:29522345(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377527629
CDS Mutation c.1161C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000380752
Start 29535841:29535841(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs573863925
CDS Mutation c.348C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000380752
Start 29532888:29532888(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749028386
CDS Mutation c.465C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000380752
Start 29535892:29535892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.297C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000380752
Start 29532954:29532954(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs538503703
CDS Mutation c.399C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000380752
Start 29517629:29517629(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1454delA
AA Mutation p.Asn485ThrfsTer10(p.N485Tfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript