Colon Cancer: Gene >> NPPB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376468
Start	11858331:11858331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377083056
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Cys(p.R91C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376468
Start	11858742:11858742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.92G>T
AA Mutation	p.Ser31Ile(p.S31I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376468
Start	11858247:11858247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750160819
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Trp(p.R119W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376468
Start	11858287:11858287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315G>T
AA Mutation	p.Lys105Asn(p.K105N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376468
Start	11858350:11858350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780193664
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376468
Start	11858714:11858714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140816420
CDS Mutation	c.120G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NPPB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376468
Start	11858330:11858330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143526178
CDS Mutation	c.272G>A
AA Mutation	p.Arg91His(p.R91H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376468
Start	11858822:11858822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12G>T
AA Mutation	p.Gln4His(p.Q4H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript