Colon Cancer: Gene >> RPL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202773
Start	112405951:112405951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616G>A
AA Mutation	p.Val206Ile(p.V206I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000202773
Start	112406833:112406833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>A
AA Mutation	p.Pro132Thr(p.P132T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000202773
Start	112405989:112405989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578T>G
AA Mutation	p.Phe193Cys(p.F193C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202773
Start	112406825:112406825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202773
Start	112405856:112405857(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.710_711delAA
AA Mutation	p.Lys237ArgfsTer4(p.K237Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RPL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202773
Start	112405989:112405989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578T>G
AA Mutation	p.Phe193Cys(p.F193C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000202773
Start	112405929:112405929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638C>T
AA Mutation	p.Thr213Ile(p.T213I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript