Primary Site >> Stomach Cancer

Gene >> NAT10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000257829
Start 34124378:34124378(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1085G>A
AA Mutation p.Arg362Gln(p.R362Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000257829
Start 34143477:34143477(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2918A>G
AA Mutation p.Asn973Ser(p.N973S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000257829
Start 34139270:34139270(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2291T>C
AA Mutation p.Leu764Pro(p.L764P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000257829
Start 34122484:34122484(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.806A>T
AA Mutation p.Glu269Val(p.E269V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000257829
Start 34112207:34112207(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.356G>C
AA Mutation p.Gly119Ala(p.G119A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000257829
Start 34115823:34115823(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.496G>A
AA Mutation p.Asp166Asn(p.D166N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000257829
Start 34108750:34108750(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.117A>G
AA Mutation p.Ile39Met(p.I39M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000257829
Start 34141799:34141799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2793G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000257829
Start 34136760:34136760(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2151delC
AA Mutation p.Arg718GlyfsTer16(p.R718Gfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000257829
Start 34108235:34108235(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.14delA
AA Mutation p.Lys5ArgfsTer14(p.K5Rfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript