Primary Site >> Stomach Cancer

Gene >> PCDHB9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141189489:141189489(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2171G>A
AA Mutation p.Arg724His(p.R724H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141189219:141189219(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1901A>G
AA Mutation p.Asp634Gly(p.D634G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141189653:141189653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2335G>T
AA Mutation p.Gly779Cys(p.G779C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141189495:141189495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2177C>T
AA Mutation p.Ser726Leu(p.S726L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141188961:141188961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1643G>A
AA Mutation p.Arg548His(p.R548H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141189332:141189332(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2014C>T
AA Mutation p.Pro672Ser(p.P672S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141189488:141189488(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2170C>T
AA Mutation p.Arg724Cys(p.R724C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141189447:141189447(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2129C>T
AA Mutation p.Ala710Val(p.A710V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141187728:141187728(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.410A>C
AA Mutation p.Glu137Ala(p.E137A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141187875:141187875(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.557A>G
AA Mutation p.Asp186Gly(p.D186G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141188907:141188907(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1589G>A
AA Mutation p.Arg530His(p.R530H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141188687:141188687(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1369A>G
AA Mutation p.Thr457Ala(p.T457A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141188957:141188957(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1639G>A
AA Mutation p.Val547Met(p.V547M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141188850:141188850(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1532G>A
AA Mutation p.Gly511Asp(p.G511D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000316105
Start 141189531:141189531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2213A>G
AA Mutation p.Asp738Gly(p.D738G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000316105
Start 141189025:141189025(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1707C>T
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000316105
Start 141188515:141188515(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1197T>C
Mutation Classification Silent
Feature Type Transcript
ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000316105
Start 141189532:141189532(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2214C>T
Mutation Classification Silent
Feature Type Transcript
ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000316105
Start 141189217:141189217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1899C>T
Mutation Classification Silent
Feature Type Transcript
ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000316105
Start 141189283:141189283(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1965C>A
Mutation Classification Silent
Feature Type Transcript
ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000316105
Start 141188953:141188953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1635G>A
Mutation Classification Silent
Feature Type Transcript
ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000316105
Start 141188159:141188159(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.846delT
AA Mutation p.Phe282LeufsTer8(p.F282Lfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 23
Mutation Consequence frameshift_variant
Transcription ID ENST00000316105
Start 141187738:141187738(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.424delA
AA Mutation p.Ile142TyrfsTer13(p.I142Yfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript