Primary Site >> Stomach Cancer

Gene >> NR3C1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000343796
Start 143281987:143281987(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2236A>G
AA Mutation p.Ser746Gly(p.S746G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000343796
Start 143399765:143399765(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370839677
CDS Mutation c.1075G>A
AA Mutation p.Val359Ile(p.V359I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000343796
Start 143310147:143310147(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1418G>T
AA Mutation p.Cys473Phe(p.C473F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000343796
Start 143282031:143282031(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2192A>C
AA Mutation p.Asn731Thr(p.N731T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000343796
Start 143282672:143282672(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2077T>G
AA Mutation p.Tyr693Asp(p.Y693D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000343796
Start 143399710:143399710(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745857266
CDS Mutation c.1130C>T
AA Mutation p.Ser377Phe(p.S377F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000343796
Start 143400733:143400733(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750532455
CDS Mutation c.107G>T
AA Mutation p.Gly36Val(p.G36V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000343796
Start 143310124:143310124(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1441T>A
AA Mutation p.Cys481Ser(p.C481S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000343796
Start 143400465:143400465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.375C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000343796
Start 143400103:143400104(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.736_737insTTTGAAGGGCC
AA Mutation p.Lys246IlefsTer2(p.K246Ifs*2)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000343796
Start 143400105:143400106(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.734_735insATGTATCTTCAGAACAGCAA
AA Mutation p.Cys245Ter(p.C245*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000343796
Start 143314065:143314065(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1288G>T
AA Mutation p.Gly430Ter(p.G430*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript