Colon Cancer: Gene >> PIR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380420
Start	15425917:15425917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554C>T
AA Mutation	p.Pro185Leu(p.P185L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380420
Start	15455880:15455880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.448G>A
AA Mutation	p.Ala150Thr(p.A150T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380420
Start	15397519:15397519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.623C>T
AA Mutation	p.Ala208Val(p.A208V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380420
Start	15397464:15397464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380420
Start	15397527:15397527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554199837
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380420
Start	15479804:15479804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138682621
CDS Mutation	c.114G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PIR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380420
Start	15455933:15455933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.395A>G
AA Mutation	p.Gln132Arg(p.Q132R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380420
Start	15456040:15456040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript