Colon Cancer: Gene >> EPS8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281172
Start	15662079:15662079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757C>A
AA Mutation	p.His253Asn(p.H253N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281172
Start	15650957:15650957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147224631
CDS Mutation	c.1300C>T
AA Mutation	p.Arg434Cys(p.R434C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281172
Start	15623249:15623249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2264T>C
AA Mutation	p.Leu755Pro(p.L755P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281172
Start	15624306:15624306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775283555
CDS Mutation	c.2146G>A
AA Mutation	p.Val716Met(p.V716M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281172
Start	15658119:15658119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061C>T
AA Mutation	p.Ala354Val(p.A354V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281172
Start	15669458:15669458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>A
AA Mutation	p.Leu149Ile(p.L149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281172
Start	15631488:15631488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1998C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EPS8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281172
Start	15669720:15669720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310G>T
AA Mutation	p.Asp104Tyr(p.D104Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281172
Start	15654216:15654216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179C>A
AA Mutation	p.Phe393Leu(p.F393L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281172
Start	15665853:15665853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript