Primary Site >> Stomach Cancer

Gene >> VCAM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000294728
Start 100734697:100734697(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777392031
CDS Mutation c.1988C>T
AA Mutation p.Ala663Val(p.A663V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000294728
Start 100738258:100738258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2195T>C
AA Mutation p.Val732Ala(p.V732A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000294728
Start 100738131:100738131(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2068A>C
AA Mutation p.Asn690His(p.N690H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000294728
Start 100729373:100729373(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1195G>A
AA Mutation p.Glu399Lys(p.E399K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000294728
Start 100731498:100731498(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780212367
CDS Mutation c.1505C>T
AA Mutation p.Thr502Met(p.T502M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000294728
Start 100720637:100720637(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.226A>G
AA Mutation p.Thr76Ala(p.T76A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000294728
Start 100720531:100720531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.120T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000294728
Start 100732560:100732560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1668G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000294728
Start 100731286:100731286(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1293C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000294728
Start 100738137:100738138(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2075_2076delAA
AA Mutation p.Lys692ArgfsTer6(p.K692Rfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript