Colon Cancer: Gene >> EDIL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84060362:84060362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075G>A
AA Mutation	p.Asp359Asn(p.D359N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84106717:84106717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Cys(p.R195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84106773:84106773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527C>A
AA Mutation	p.Ala176Asp(p.A176D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84064834:84064834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818G>A
AA Mutation	p.Gly273Glu(p.G273E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	83963270:83963270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1228C>G
AA Mutation	p.Leu410Val(p.L410V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	83943543:83943543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319A>G
AA Mutation	p.Asp440Gly(p.D440G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84106684:84106684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616A>G
AA Mutation	p.Thr206Ala(p.T206A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84254120:84254120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160T>G
AA Mutation	p.Phe54Val(p.F54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296591
Start	83943521:83943521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747340278
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296591
Start	84064734:84064734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.918T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296591
Start	84060303:84060303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752216203
CDS Mutation	c.1134A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296591
Start	84064788:84064788(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.864delC
AA Mutation	p.Ile289Ter(p.I289*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EDIL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84106717:84106717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Cys(p.R195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84106747:84106747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>A
AA Mutation	p.Gly185Arg(p.G185R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84254126:84254126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.154G>C
AA Mutation	p.Asp52His(p.D52H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296591
Start	84137338:84137338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372A>C
AA Mutation	p.Glu124Asp(p.E124D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296591
Start	84137278:84137278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432G>A
Mutation Classification	Silent
Feature Type	Transcript