Primary Site >> Stomach Cancer

Gene >> BORA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000613797
Start 72729075:72729075(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.360T>A
AA Mutation p.Phe120Leu(p.F120L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000613797
Start 72746605:72746605(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1201C>T
AA Mutation p.Pro401Ser(p.P401S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000613797
Start 72738015:72738015(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.585A>C
AA Mutation p.Lys195Asn(p.K195N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000613797
Start 72746061:72746061(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753266386
CDS Mutation c.1081G>C
AA Mutation p.Glu361Gln(p.E361Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000613797
Start 72746019:72746019(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1039A>G
AA Mutation p.Ile347Val(p.I347V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000613797
Start 72746704:72746704(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1300G>T
AA Mutation p.Gly434Cys(p.G434C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000613797
Start 72747056:72747056(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1652G>A
AA Mutation p.Cys551Tyr(p.C551Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000613797
Start 72729012:72729012(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.297T>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000613797
Start 72745979:72745979(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1005delA
AA Mutation p.Lys335AsnfsTer7(p.K335Nfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000613797
Start 72753720:72753720(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1738G>T
AA Mutation p.Gly580Ter(p.G580*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript