Primary Site >> Stomach Cancer

Gene >> DTNA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000399113
Start 34812029:34812029(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.519A>C
AA Mutation p.Glu173Asp(p.E173D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000399113
Start 34875342:34875342(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199556035
CDS Mutation c.1766C>T
AA Mutation p.Thr589Met(p.T589M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000399113
Start 34851923:34851923(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1446G>T
AA Mutation p.Lys482Asn(p.K482N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000399113
Start 34851876:34851876(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144880521
CDS Mutation c.1399G>A
AA Mutation p.Asp467Asn(p.D467N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000399113
Start 34864004:34864004(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1604T>C
AA Mutation p.Leu535Pro(p.L535P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000399113
Start 34818312:34818312(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.858G>A
AA Mutation p.Met286Ile(p.M286I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000399113
Start 34879650:34879650(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747872788
CDS Mutation c.2012C>T
AA Mutation p.Ala671Val(p.A671V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000399113
Start 34766037:34766037(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.144C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000399113
Start 34875352:34875352(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1776C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000399113
Start 34875368:34875368(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1796delG
AA Mutation p.Gly599GlufsTer15(p.G599Efs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript