Colon Cancer: Gene >> MRPL16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300151
Start	59806606:59806606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370177555
CDS Mutation	c.497G>A
AA Mutation	p.Arg166His(p.R166H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300151
Start	59807757:59807757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214A>G
AA Mutation	p.Ile72Val(p.I72V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300151
Start	59806430:59806430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673G>A
AA Mutation	p.Gly225Ser(p.G225S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300151
Start	59806511:59806511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592A>G
AA Mutation	p.Met198Val(p.M198V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300151
Start	59806653:59806653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146680546
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300151
Start	59806497:59806497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000300151
Start	59806508:59806508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779032152
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Ter(p.R199*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	start_lost
Transcription ID	ENST00000300151
Start	59810656:59810656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MRPL16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300151
Start	59806523:59806523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580A>G
AA Mutation	p.Thr194Ala(p.T194A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript