Colon Cancer: Gene >> EID3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000527879
Start	104304900:104304900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966A>C
AA Mutation	p.Glu322Asp(p.E322D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000527879
Start	104304199:104304199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265G>A
AA Mutation	p.Asp89Asn(p.D89N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000527879
Start	104304686:104304686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.752C>A
AA Mutation	p.Ser251Tyr(p.S251Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000527879
Start	104304055:104304055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377416878
CDS Mutation	c.121C>T
AA Mutation	p.Arg41Cys(p.R41C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000527879
Start	104304047:104304047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774171990
CDS Mutation	c.113G>A
AA Mutation	p.Arg38His(p.R38H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000527879
Start	104304595:104304595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751970447
CDS Mutation	c.661G>A
AA Mutation	p.Val221Ile(p.V221I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000527879
Start	104304085:104304085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151G>A
AA Mutation	p.Val51Met(p.V51M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EID3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000527879
Start	104304815:104304815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881G>A
AA Mutation	p.Gly294Glu(p.G294E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000527879
Start	104304488:104304488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.554G>A
AA Mutation	p.Arg185Gln(p.R185Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript