Primary Site >> Stomach Cancer

Gene >> NKX6-2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368592
Start 132785073:132785073(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.677A>G
AA Mutation p.Lys226Arg(p.K226R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368592
Start 132785001:132785001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.749A>C
AA Mutation p.Lys250Thr(p.K250T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368592
Start 132785375:132785375(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776578386
CDS Mutation c.484G>A
AA Mutation p.Ala162Thr(p.A162T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368592
Start 132785315:132785315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.544G>A
AA Mutation p.Ala182Thr(p.A182T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368592
Start 132785804:132785804(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.145G>T
AA Mutation p.Gly49Cys(p.G49C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000368592
Start 132785307:132785307(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.552G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000368592
Start 132784934:132784934(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.816C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000368592
Start 132785358:132785358(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.501C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000368592
Start 132784927:132784927(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.823delG
AA Mutation p.Asp275ThrfsTer32(p.D275Tfs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript