Colon Cancer: Gene >> PPIE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324379
Start	39743866:39743866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764879686
CDS Mutation	c.326C>T
AA Mutation	p.Thr109Met(p.T109M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324379
Start	39745472:39745472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776933148
CDS Mutation	c.482G>A
AA Mutation	p.Arg161His(p.R161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324379
Start	39749080:39749080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747872958
CDS Mutation	c.686C>T
AA Mutation	p.Thr229Met(p.T229M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324379
Start	39740186:39740186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53A>G
AA Mutation	p.Asp18Gly(p.D18G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324379
Start	39749067:39749067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673A>G
AA Mutation	p.Ile225Val(p.I225V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324379
Start	39743246:39743246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Cys(p.R78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324379
Start	39749051:39749051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758344472
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324379
Start	39749081:39749081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757552287
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372830
Start	39762558:39762558(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.884delA
AA Mutation	p.Asn295ThrfsTer46(p.N295Tfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPIE

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324379
Start	39743251:39743251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237C>A
Mutation Classification	Silent
Feature Type	Transcript