Colon Cancer: Gene >> EPHX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370383
Start	92063119:92063119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373441880
CDS Mutation	c.922G>A
AA Mutation	p.Ala308Thr(p.A308T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370383
Start	92063237:92063237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040A>G
AA Mutation	p.Asn347Ser(p.N347S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370383
Start	92032584:92032584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311A>G
AA Mutation	p.Glu104Gly(p.E104G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370383
Start	92032586:92032586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313T>A
AA Mutation	p.Phe105Ile(p.F105I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370383
Start	92052598:92052598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797A>G
AA Mutation	p.Tyr266Cys(p.Y266C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EPHX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370383
Start	92042828:92042828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323C>A
AA Mutation	p.Ser108Tyr(p.S108Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370383
Start	92045633:92045633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577A>C
AA Mutation	p.Asn193His(p.N193H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript