Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> AADAC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000232892
Start 151827675:151827675(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.703A>C
AA Mutation p.Asn235His(p.N235H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000232892
Start 151828130:151828130(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1158A>C
AA Mutation p.Arg386Ser(p.R386S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000232892
Start 151824713:151824713(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.482A>G
AA Mutation p.Tyr161Cys(p.Y161C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000232892
Start 151827626:151827626(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.654T>G
AA Mutation p.Ile218Met(p.I218M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000232892
Start 151827619:151827619(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.647C>T
AA Mutation p.Ser216Phe(p.S216F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000232892
Start 151827927:151827927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.955G>A
AA Mutation p.Ala319Thr(p.A319T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000232892
Start 151827730:151827730(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.758delA
AA Mutation p.Tyr253PhefsTer40(p.Y253Ffs*40)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000232892
Start 151827905:151827905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.933T>A
AA Mutation p.Tyr311Ter(p.Y311*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> AADAC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000232892
Start 151827796:151827796(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.824G>T
AA Mutation p.Ser275Ile(p.S275I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000232892
Start 151827743:151827743(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756745068
CDS Mutation c.771T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 3
Mutation Consequence stop_gained
Transcription ID ENST00000232892
Start 151828145:151828145(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1173T>G
AA Mutation p.Tyr391Ter(p.Y391*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript