Colon Cancer: Gene >> SH3GLB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370558
Start	86742285:86742285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839G>A
AA Mutation	p.Gly280Asp(p.G280D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370558
Start	86743231:86743231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094A>G
AA Mutation	p.Asn365Ser(p.N365S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370558
Start	86734610:86734610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.579G>T
AA Mutation	p.Gln193His(p.Q193H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370558
Start	86719580:86719580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000370558
Start	86722596:86722596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>T
AA Mutation	p.Glu134Ter(p.E134*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000370558
Start	86719521:86719521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229G>T
AA Mutation	p.Glu77Ter(p.E77*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SH3GLB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370558
Start	86722623:86722623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427T>G
AA Mutation	p.Phe143Val(p.F143V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript