Primary Site >> Stomach Cancer

Gene >> CASP10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000272879
Start 201209460:201209460(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1313T>G
AA Mutation p.Leu438Arg(p.L438R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000272879
Start 201195880:201195880(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.616G>A
AA Mutation p.Glu206Lys(p.E206K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000272879
Start 201209201:201209201(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762087406
CDS Mutation c.1054G>A
AA Mutation p.Val352Met(p.V352M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000272879
Start 201186066:201186066(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.289T>C
AA Mutation p.Cys97Arg(p.C97R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000272879
Start 201209247:201209247(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774726645
CDS Mutation c.1100C>T
AA Mutation p.Ser367Leu(p.S367L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000272879
Start 201229018:201229018(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1501C>A
AA Mutation p.Leu501Met(p.L501M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000272879
Start 201205885:201205885(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.725A>C
AA Mutation p.Asn242Thr(p.N242T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000272879
Start 201185870:201185870(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.97delG
AA Mutation p.Val33SerfsTer12(p.V33Sfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript