Primary Site >> Stomach Cancer

Gene >> NKX2-1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000498187
Start 36517916:36517916(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.478C>A
AA Mutation p.Pro160Thr(p.P160T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000498187
Start 36517796:36517796(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.598C>A
AA Mutation p.Leu200Met(p.L200M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000498187
Start 36519012:36519012(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.346G>A
AA Mutation p.Ala116Thr(p.A116T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000498187
Start 36517919:36517919(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.475G>A
AA Mutation p.Ala159Thr(p.A159T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000498187
Start 36519181:36519181(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.177G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000498187
Start 36517971:36517971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.423C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000498187
Start 36517998:36517998(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.396G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000498187
Start 36517794:36517794(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.600G>A
Mutation Classification Silent
Feature Type Transcript