Colon Cancer: Gene >> NPPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376480
Start	11847391:11847391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768114654
CDS Mutation	c.172G>A
AA Mutation	p.Val58Met(p.V58M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376480
Start	11847186:11847186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1803268
CDS Mutation	c.377G>A
AA Mutation	p.Arg126Gln(p.R126Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376480
Start	11847582:11847582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202145205
CDS Mutation	c.103G>A
AA Mutation	p.Ala35Thr(p.A35T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376480
Start	11847639:11847639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754947478
CDS Mutation	c.46G>A
AA Mutation	p.Ala16Thr(p.A16T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376480
Start	11847272:11847272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000376480
Start	11847440:11847440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NPPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376480
Start	11847199:11847199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364C>A
AA Mutation	p.Pro122Thr(p.P122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000376480
Start	11847440:11847440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript