Primary Site >> Stomach Cancer

Gene >> SERPINB3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000283752
Start 63655694:63655694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1136A>C
AA Mutation p.Asn379Thr(p.N379T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000283752
Start 63655869:63655869(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs540991572
CDS Mutation c.961C>T
AA Mutation p.Arg321Cys(p.R321C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000283752
Start 63659497:63659497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.253T>A
AA Mutation p.Phe85Ile(p.F85I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000283752
Start 63659415:63659415(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140004752
CDS Mutation c.335C>T
AA Mutation p.Thr112Met(p.T112M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000283752
Start 63655876:63655876(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753692328
CDS Mutation c.954C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000283752
Start 63655696:63655696(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1134C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000283752
Start 63655867:63655867(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763567283
CDS Mutation c.963C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000283752
Start 63659426:63659426(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376584936
CDS Mutation c.324C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000283752
Start 63659402:63659402(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.348A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000283752
Start 63659403:63659403(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.347delT
AA Mutation p.Leu116TyrfsTer5(p.L116Yfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000283752
Start 63655850:63655850(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.980delG
AA Mutation p.Gly327GlufsTer23(p.G327Efs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence inframe_insertion
Transcription ID ENST00000283752
Start 63657383:63657384(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.493_498dupGAAGGT
AA Mutation p.Glu165_Gly166dup(p.E165_G166dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript