Colon Cancer: Gene >> XPNPEP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357137
Start	40881967:40881967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379T>A
AA Mutation	p.Phe127Ile(p.F127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357137
Start	40914254:40914254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985C>T
AA Mutation	p.Leu329Phe(p.L329F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357137
Start	40909191:40909191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769806045
CDS Mutation	c.925C>T
AA Mutation	p.Arg309Trp(p.R309W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357137
Start	40924482:40924482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357G>A
AA Mutation	p.Gly453Ser(p.G453S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357137
Start	40907638:40907638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844C>A
AA Mutation	p.Leu282Ile(p.L282I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357137
Start	40926329:40926329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757967685
CDS Mutation	c.1418G>A
AA Mutation	p.Arg473Gln(p.R473Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357137
Start	40881812:40881812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769655576
CDS Mutation	c.224G>A
AA Mutation	p.Arg75His(p.R75H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000357137
Start	40926328:40926328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1417C>T
AA Mutation	p.Arg473Ter(p.R473*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	start_lost
Transcription ID	ENST00000357137
Start	40857184:40857184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> XPNPEP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357137
Start	40922446:40922446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1169C>T
AA Mutation	p.Thr390Ile(p.T390I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357137
Start	40909155:40909155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889A>G
AA Mutation	p.Ile297Val(p.I297V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript