Colon Cancer: Gene >> PES1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354694
Start	30580170:30580170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052G>A
AA Mutation	p.Gly351Asp(p.G351D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354694
Start	30580068:30580068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154C>T
AA Mutation	p.Thr385Ile(p.T385I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354694
Start	30584709:30584709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377C>T
AA Mutation	p.Thr126Met(p.T126M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354694
Start	30578920:30578920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1600C>A
AA Mutation	p.Arg534Ser(p.R534S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354694
Start	30577096:30577096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750124332
CDS Mutation	c.1717G>A
AA Mutation	p.Asp573Asn(p.D573N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354694
Start	30587333:30587333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321A>C
AA Mutation	p.Leu107Phe(p.L107F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354694
Start	30581055:30581055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869C>T
AA Mutation	p.Ala290Val(p.A290V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354694
Start	30581533:30581533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742C>A
AA Mutation	p.Pro248Thr(p.P248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354694
Start	30581531:30581531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147244950
CDS Mutation	c.744G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000354694
Start	30580653:30580653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961G>T
AA Mutation	p.Glu321Ter(p.E321*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PES1

No Mutation Annotation!