Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PNMT

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000269582
Start 39670070:39670070(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.530C>T
AA Mutation p.Ala177Val(p.A177V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000269582
Start 39670031:39670031(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.491C>A
AA Mutation p.Pro164His(p.P164H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000269582
Start 39670258:39670258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.718A>G
AA Mutation p.Arg240Gly(p.R240G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000269582
Start 39669780:39669780(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.358delG
AA Mutation p.Ala120ProfsTer32(p.A120Pfs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000269582
Start 39670162:39670162(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.627delG
AA Mutation p.His210ThrfsTer20(p.H210Tfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000269582
Start 39670161:39670162(version: GRCh38)
Mutation Type INS
dbSNP_RS rs771451039
CDS Mutation c.627dupG
AA Mutation p.His210AlafsTer27(p.H210Afs*27)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000269582
Start 39669628:39669628(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.203-1G>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> PNMT

No Mutation Annotation!