Primary Site >> Stomach Cancer

Gene >> CCDC110

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000307588
Start 185459910:185459910(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.677C>A
AA Mutation p.Thr226Asn(p.T226N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000307588
Start 185459117:185459117(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1470T>G
AA Mutation p.Ile490Met(p.I490M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000307588
Start 185459846:185459846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.741A>C
AA Mutation p.Gln247His(p.Q247H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000307588
Start 185461082:185461082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.315T>A
AA Mutation p.Asn105Lys(p.N105K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000307588
Start 185458339:185458339(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767005070
CDS Mutation c.2248G>A
AA Mutation p.Val750Ile(p.V750I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000307588
Start 185459562:185459562(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1025A>C
AA Mutation p.Lys342Thr(p.K342T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000307588
Start 185459452:185459452(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1135A>G
AA Mutation p.Arg379Gly(p.R379G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000307588
Start 185460000:185460000(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.587A>G
AA Mutation p.Asn196Ser(p.N196S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000307588
Start 185458340:185458340(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752180798
CDS Mutation c.2247C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000307588
Start 185458136:185458136(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751089698
CDS Mutation c.2451G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000307588
Start 185458559:185458559(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2028T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000307588
Start 185459861:185459861(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.726C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000307588
Start 185458813:185458813(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1774delA
AA Mutation p.Thr592HisfsTer5(p.T592Hfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000307588
Start 185458789:185458789(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1798delA
AA Mutation p.Ser600AlafsTer7(p.S600Afs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000307588
Start 185459320:185459320(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1267C>T
AA Mutation p.Gln423Ter(p.Q423*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000307588
Start 185458812:185458813(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1774dupA
AA Mutation p.Thr592AsnfsTer14(p.T592Nfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 17
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000307588
Start 185471050:185471050(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11-1G>C
Mutation Classification Splice_Site
Feature Type Transcript