Colon Cancer: Gene >> APOA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116821553:116821553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142295954
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Trp(p.R169W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116821475:116821475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.583G>A
AA Mutation	p.Glu195Lys(p.E195K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116821141:116821141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549843769
CDS Mutation	c.917G>A
AA Mutation	p.Arg306Gln(p.R306Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116821412:116821412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646G>A
AA Mutation	p.Val216Met(p.V216M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116821399:116821399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541515376
CDS Mutation	c.659G>A
AA Mutation	p.Arg220His(p.R220H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116821016:116821016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1042A>G
AA Mutation	p.Arg348Gly(p.R348G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116821453:116821453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147626624
CDS Mutation	c.605C>T
AA Mutation	p.Thr202Met(p.T202M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116820946:116820946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112C>A
AA Mutation	p.Pro371His(p.P371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116821552:116821552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506G>A
AA Mutation	p.Arg169Gln(p.R169Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116821225:116821225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833T>C
AA Mutation	p.Leu278Pro(p.L278P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> APOA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357780
Start	116820978:116820978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080G>T
AA Mutation	p.Glu360Asp(p.E360D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript