Primary Site >> Stomach Cancer

Gene >> DISC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000439617
Start 231771055:231771055(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143165003
CDS Mutation c.1619C>T
AA Mutation p.Pro540Leu(p.P540L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000439617
Start 232008874:232008874(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2132G>T
AA Mutation p.Arg711Met(p.R711M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000439617
Start 231694559:231694559(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.801T>G
AA Mutation p.Ser267Arg(p.S267R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000439617
Start 232008793:232008793(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2051G>T
AA Mutation p.Cys684Phe(p.C684F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000439617
Start 231818344:231818344(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148111679
CDS Mutation c.1808C>T
AA Mutation p.Thr603Met(p.T603M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000439617
Start 231694044:231694044(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.286C>T
AA Mutation p.Arg96Trp(p.R96W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000439617
Start 231818340:231818340(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1804T>C
AA Mutation p.Trp602Arg(p.W602R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000439617
Start 231770918:231770918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1482G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000439617
Start 231767230:231767230(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144844117
CDS Mutation c.1359G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000439617
Start 231694541:231694541(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.783T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000439617
Start 231770891:231770891(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1455G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000439617
Start 231750041:231750041(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1233A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000439617
Start 231770972:231770972(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1536C>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000439617
Start 231750063:231750063(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1258delG
AA Mutation p.Ala420ProfsTer14(p.A420Pfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000439617
Start 232008939:232008939(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2202delC
AA Mutation p.Arg735GlyfsTer12(p.R735Gfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000439617
Start 231694319:231694319(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.561C>A
AA Mutation p.Cys187Ter(p.C187*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000439617
Start 231818327:231818327(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1793-2A>G
Mutation Classification Splice_Site
Feature Type Transcript