Primary Site >> Stomach Cancer

Gene >> EVL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000402714
Start 100084790:100084790(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.109A>G
AA Mutation p.Asn37Asp(p.N37D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000402714
Start 100141785:100141785(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1205T>C
AA Mutation p.Ile402Thr(p.I402T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000402714
Start 100137745:100137745(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773230379
CDS Mutation c.1031C>T
AA Mutation p.Pro344Leu(p.P344L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000402714
Start 100129571:100129571(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145112596
CDS Mutation c.720C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000402714
Start 100129583:100129583(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.732C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000402714
Start 100141784:100141784(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1204delA
AA Mutation p.Ile402SerfsTer9(p.I402Sfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant
Transcription ID ENST00000402714
Start 100137646:100137646(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1025+2T>C
Mutation Classification Splice_Site
Feature Type Transcript