Primary Site >> Stomach Cancer

Gene >> ALCAM

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105547519:105547519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1370A>G
AA Mutation p.Asn457Ser(p.N457S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105534827:105534827(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.712G>A
AA Mutation p.Ala238Thr(p.A238T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105533676:105533676(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.533A>G
AA Mutation p.His178Arg(p.H178R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105552498:105552498(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1577C>T
AA Mutation p.Ala526Val(p.A526V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105524437:105524437(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.323A>C
AA Mutation p.Glu108Ala(p.E108A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105547237:105547237(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1193A>G
AA Mutation p.Glu398Gly(p.E398G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105545277:105545277(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1046C>T
AA Mutation p.Ala349Val(p.A349V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105540070:105540070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.826C>T
AA Mutation p.Pro276Ser(p.P276S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105552488:105552488(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1567A>G
AA Mutation p.Asn523Asp(p.N523D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000306107
Start 105524295:105524295(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.181C>T
AA Mutation p.Pro61Ser(p.P61S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000306107
Start 105545287:105545287(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1056G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000306107
Start 105533641:105533641(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.498C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000306107
Start 105532060:105532060(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.458delA
AA Mutation p.Lys153SerfsTer34(p.K153Sfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000306107
Start 105541726:105541726(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.958delA
AA Mutation p.Ser320AlafsTer2(p.S320Afs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript