Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NEUROG3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000242462
Start 69572668:69572668(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.376C>T
AA Mutation p.Arg126Cys(p.R126C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000242462
Start 69572722:69572722(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.322G>A
AA Mutation p.Gly108Ser(p.G108S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000242462
Start 69573016:69573016(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.28A>C
AA Mutation p.Thr10Pro(p.T10P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000242462
Start 69572643:69572643(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.401C>T
AA Mutation p.Ala134Val(p.A134V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000242462
Start 69572626:69572626(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766165230
CDS Mutation c.418C>T
AA Mutation p.Arg140Cys(p.R140C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000242462
Start 69572582:69572582(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199710370
CDS Mutation c.462G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000242462
Start 69572798:69572798(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.246G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000242462
Start 69572963:69572963(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765224454
CDS Mutation c.81C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000242462
Start 69572473:69572473(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770935946
CDS Mutation c.571C>T
AA Mutation p.Arg191Ter(p.R191*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000242462
Start 69572881:69572881(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.163C>T
AA Mutation p.Arg55Ter(p.R55*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> NEUROG3

No Mutation Annotation!