Colon Cancer: Gene >> POTED

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299443
Start	13641382:13641382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564938629
CDS Mutation	c.1571G>A
AA Mutation	p.Arg524His(p.R524H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299443
Start	13610496:13610496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268T>C
AA Mutation	p.Phe90Leu(p.F90L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299443
Start	13610583:13610583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374506316
CDS Mutation	c.355G>A
AA Mutation	p.Ala119Thr(p.A119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299443
Start	13610607:13610607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762265878
CDS Mutation	c.379G>A
AA Mutation	p.Ala127Thr(p.A127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299443
Start	13620217:13620217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.977A>G
AA Mutation	p.Glu326Gly(p.E326G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000299443
Start	13641498:13641498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1687G>T
AA Mutation	p.Glu563Ter(p.E563*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> POTED

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299443
Start	13610702:13610702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript