Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EIF4A2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000323963
Start 186787870:186787870(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1067A>C
AA Mutation p.Asn356Thr(p.N356T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000323963
Start 186789201:186789201(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1156C>G
AA Mutation p.Arg386Gly(p.R386G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000323963
Start 186787875:186787875(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1072A>G
AA Mutation p.Ile358Val(p.I358V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000323963
Start 186789201:186789201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1156C>A
AA Mutation p.Arg386Ser(p.R386S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000323963
Start 186786269:186786270(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.623_624insACTGTCATTTCTAGATCTAC
AA Mutation p.Gln209LeufsTer23(p.Q209Lfs*23)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 6
Mutation Consequence inframe_deletion
Transcription ID ENST00000323963
Start 186785996:186785998(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs767682413
CDS Mutation c.463_465delATT
AA Mutation p.Ile155del(p.I155del)
Mutation Classification In_Frame_Del
Feature Type Transcript

Rectum Cancer: Gene >> EIF4A2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000323963
Start 186789141:186789141(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1096C>G
AA Mutation p.Arg366Gly(p.R366G)
Mutation Classification Missense_Mutation
Feature Type Transcript