Colon Cancer: Gene >> RPL7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352983
Start	73292260:73292260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269C>T
AA Mutation	p.Ala90Val(p.A90V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352983
Start	73291123:73291123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668A>G
AA Mutation	p.Lys223Arg(p.K223R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000352983
Start	73291621:73291621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Cys(p.R157C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352983
Start	73292747:73292747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65G>A
AA Mutation	p.Arg22Gln(p.R22Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000352983
Start	73292694:73292694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118A>C
AA Mutation	p.Lys40Gln(p.K40Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352983
Start	73292737:73292737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754441231
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RPL7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352983
Start	73292401:73292401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128G>A
AA Mutation	p.Arg43Gln(p.R43Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript