Primary Site >> Stomach Cancer

Gene >> PTGER3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306666
Start 71047550:71047550(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.28G>A
AA Mutation p.Asp10Asn(p.D10N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306666
Start 71047445:71047445(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757690899
CDS Mutation c.133G>A
AA Mutation p.Glu45Lys(p.E45K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306666
Start 71046927:71046927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.651C>A
AA Mutation p.Asn217Lys(p.N217K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000356595
Start 70952973:70952973(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1191A>T
AA Mutation p.Glu397Asp(p.E397D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000356595
Start 70952928:70952928(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1236C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000306666
Start 71046966:71046966(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755813776
CDS Mutation c.612C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000306666
Start 71012440:71012440(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.942C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000306666
Start 71047215:71047215(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.363G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000306666
Start 71047437:71047437(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.141C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000356595
Start 70952919:70952919(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1245A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000306666
Start 71046938:71046938(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.640C>T
AA Mutation p.Arg214Ter(p.R214*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript