Colon Cancer: Gene >> REN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272190
Start	204156738:204156738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267598319
CDS Mutation	c.757G>A
AA Mutation	p.Glu253Lys(p.E253K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272190
Start	204155155:204155155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1082T>A
AA Mutation	p.Leu361Gln(p.L361Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272190
Start	204155912:204155912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745900131
CDS Mutation	c.967G>A
AA Mutation	p.Val323Met(p.V323M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272190
Start	204155107:204155107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130C>A
AA Mutation	p.Pro377His(p.P377H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272190
Start	204156278:204156278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>T
AA Mutation	p.Cys287Phe(p.C287F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000272190
Start	204159521:204159521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567G>T
AA Mutation	p.Glu189Asp(p.E189D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000272190
Start	204160661:204160661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>A
AA Mutation	p.Asp131Asn(p.D131N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272190
Start	204156187:204156187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272190
Start	204162064:204162064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272190
Start	204161381:204161381(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.284delC
AA Mutation	p.Pro95HisfsTer76(p.P95Hfs*76)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> REN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272190
Start	204155077:204155077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371478505
CDS Mutation	c.1160G>A
AA Mutation	p.Arg387Gln(p.R387Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272190
Start	204156193:204156193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945G>T
AA Mutation	p.Lys315Asn(p.K315N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript