Colon Cancer: Gene >> CPA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296046
Start	148869031:148869031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261G>T
AA Mutation	p.Met87Ile(p.M87I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296046
Start	148879882:148879882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569T>C
AA Mutation	p.Val190Ala(p.V190A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296046
Start	148883799:148883799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.965C>G
AA Mutation	p.Pro322Arg(p.P322R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296046
Start	148878698:148878698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Cys(p.R142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296046
Start	148878444:148878444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746693413
CDS Mutation	c.273C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CPA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296046
Start	148868976:148868976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753756118
CDS Mutation	c.206G>A
AA Mutation	p.Arg69Gln(p.R69Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript