Primary Site >> Stomach Cancer

Gene >> CPVL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265394
Start 29092672:29092672(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs572392082
CDS Mutation c.493A>G
AA Mutation p.Thr165Ala(p.T165A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265394
Start 29096190:29096190(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.316C>A
AA Mutation p.Leu106Ile(p.L106I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000265394
Start 29095140:29095140(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750931528
CDS Mutation c.406C>T
AA Mutation p.Arg136Cys(p.R136C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000265394
Start 29066024:29066024(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376043843
CDS Mutation c.962C>T
AA Mutation p.Thr321Met(p.T321M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000265394
Start 29096215:29096215(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.291A>G
AA Mutation p.Ile97Met(p.I97M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265394
Start 29071895:29071895(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs540733056
CDS Mutation c.742G>A
AA Mutation p.Gly248Ser(p.G248S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000265394
Start 29071843:29071843(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.794delA
AA Mutation p.Lys265SerfsTer11(p.K265Sfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000265394
Start 29030646:29030646(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1251delA
AA Mutation p.Val418PhefsTer24(p.V418Ffs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript