Colon Cancer: Gene >> MRPL13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306185
Start	120414100:120414100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406G>A
AA Mutation	p.Asp136Asn(p.D136N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000306185
Start	120419938:120419938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307A>G
AA Mutation	p.Ile103Val(p.I103V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306185
Start	120432042:120432042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233C>T
AA Mutation	p.Ser78Phe(p.S78F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306185
Start	120419911:120419911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306185
Start	120419901:120419901(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.344delA
AA Mutation	p.Asn115ThrfsTer7(p.N115Tfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306185
Start	120414084:120414085(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.421_422insGTAGG
AA Mutation	p.Leu141CysfsTer3(p.L141Cfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MRPL13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306185
Start	120425343:120425343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269T>G
AA Mutation	p.Val90Gly(p.V90G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000306185
Start	120432124:120432124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript