Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TEAD4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359864
Start 3038067:3038067(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.997A>G
AA Mutation p.Lys333Glu(p.K333E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359864
Start 3021853:3021853(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.733C>T
AA Mutation p.His245Tyr(p.H245Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359864
Start 3020657:3020657(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371373848
CDS Mutation c.607G>A
AA Mutation p.Ala203Thr(p.A203T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359864
Start 2994836:2994836(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs527238579
CDS Mutation c.70G>A
AA Mutation p.Ala24Thr(p.A24T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359864
Start 3018576:3018576(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.515G>A
AA Mutation p.Gly172Glu(p.G172E)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> TEAD4

Mutation ID 1
Mutation Consequence stop_gained
Transcription ID ENST00000359864
Start 3038067:3038067(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.997A>T
AA Mutation p.Lys333Ter(p.K333*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript