Primary Site >> Stomach Cancer

Gene >> TLX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370196
Start 101136884:101136884(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.964G>A
AA Mutation p.Val322Ile(p.V322I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370196
Start 101136789:101136789(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.869C>T
AA Mutation p.Pro290Leu(p.P290L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370196
Start 101131657:101131657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.116G>A
AA Mutation p.Arg39His(p.R39H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370196
Start 101134235:101134235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.629G>A
AA Mutation p.Arg210His(p.R210H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000370196
Start 101136853:101136853(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.933G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000370196
Start 101134197:101134197(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.591G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000370196
Start 101134198:101134198(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.597delC
AA Mutation p.Lys200ArgfsTer41(p.K200Rfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript