Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MRPL19

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000393909
Start 75652145:75652145(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.225C>A
AA Mutation p.Phe75Leu(p.F75L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000393909
Start 75646881:75646881(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.74T>C
AA Mutation p.Leu25Pro(p.L25P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000393909
Start 75647166:75647166(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.168G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000393909
Start 75646885:75646885(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.83delC
AA Mutation p.Pro28ArgfsTer49(p.P28Rfs*49)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000393909
Start 75646884:75646885(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.83dupC
AA Mutation p.Pro29AlafsTer51(p.P29Afs*51)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 6
Mutation Consequence splice_donor_variant
Transcription ID ENST00000393909
Start 75652659:75652659(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.475+2T>C
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> MRPL19

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000393909
Start 75652212:75652212(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.292G>T
AA Mutation p.Asp98Tyr(p.D98Y)
Mutation Classification Missense_Mutation
Feature Type Transcript