Primary Site >> Esophagus Cancer

Gene >> TFPI2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000222543
Start 93886845:93886845(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149215949
CDS Mutation c.683G>A
AA Mutation p.Arg228Gln(p.R228Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000222543
Start 93890223:93890223(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.185G>T
AA Mutation p.Arg62Leu(p.R62L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000222543
Start 93890645:93890645(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.34C>A
AA Mutation p.Leu12Met(p.L12M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000222543
Start 93890223:93890223(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.185G>A
AA Mutation p.Arg62His(p.R62H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000222543
Start 93889163:93889163(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.332A>G
AA Mutation p.Glu111Gly(p.E111G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000222543
Start 93890311:93890311(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.97G>A
AA Mutation p.Ala33Thr(p.A33T)
Mutation Classification Missense_Mutation
Feature Type Transcript