Primary Site >> Stomach Cancer

Gene >> NAT2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000286479
Start 18400581:18400581(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs79050330
CDS Mutation c.578C>T
AA Mutation p.Thr193Met(p.T193M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000286479
Start 18400202:18400202(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201345576
CDS Mutation c.199T>C
AA Mutation p.Trp67Arg(p.W67R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000286479
Start 18400554:18400554(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.551A>C
AA Mutation p.Lys184Thr(p.K184T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000286479
Start 18400348:18400348(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs45532639
CDS Mutation c.345C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000286479
Start 18400345:18400345(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.342T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000286479
Start 18400837:18400837(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.834T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000286479
Start 18400569:18400569(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.566delT
AA Mutation p.Ile189AsnfsTer17(p.I189Nfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript