Colon Cancer: Gene >> EMX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000553456
Start	117545698:117545698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473G>A
AA Mutation	p.Arg158Gln(p.R158Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000553456
Start	117548120:117548120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647A>G
AA Mutation	p.Glu216Gly(p.E216G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000553456
Start	117545635:117545635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410A>G
AA Mutation	p.Asn137Ser(p.N137S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000553456
Start	117548066:117548066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593T>C
AA Mutation	p.Val198Ala(p.V198A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553456
Start	117548136:117548136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553456
Start	117543405:117543405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.138G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EMX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000553456
Start	117545703:117545703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478G>A
AA Mutation	p.Ala160Thr(p.A160T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000553456
Start	117545651:117545651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.426G>T
AA Mutation	p.Glu142Asp(p.E142D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000553456
Start	117545772:117545772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547G>A
AA Mutation	p.Glu183Lys(p.E183K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript