Primary Site >> Stomach Cancer

Gene >> PAM

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000438793
Start 102949968:102949968(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.791A>C
AA Mutation p.Gln264Pro(p.Q264P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000438793
Start 102960024:102960024(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1055A>G
AA Mutation p.Lys352Arg(p.K352R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000438793
Start 102948401:102948401(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.599A>G
AA Mutation p.Tyr200Cys(p.Y200C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000438793
Start 102990352:102990352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1564A>G
AA Mutation p.Lys522Glu(p.K522E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000438793
Start 102974241:102974241(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1288G>T
AA Mutation p.Val430Phe(p.V430F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000438793
Start 102913992:102913992(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.327C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000438793
Start 103025231:103025231(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs576022176
CDS Mutation c.2586G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000438793
Start 102926649:102926649(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.507G>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000438793
Start 102974245:102974245(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1298delA
AA Mutation p.Lys433ArgfsTer32(p.K433Rfs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000438793
Start 103025313:103025313(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2673delA
AA Mutation p.Lys891AsnfsTer31(p.K891Nfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000438793
Start 102901383:102901383(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.238C>T
AA Mutation p.Arg80Ter(p.R80*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000438793
Start 103003140:103003141(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1727dupA
AA Mutation p.Asn576LysfsTer13(p.N576Kfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript