Colon Cancer: Gene >> MAPRE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233121
Start	27026289:27026289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.787G>A
AA Mutation	p.Ala263Thr(p.A263T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233121
Start	27024202:27024202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374A>G
AA Mutation	p.Asn125Ser(p.N125S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233121
Start	27025923:27025923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766068888
CDS Mutation	c.668G>A
AA Mutation	p.Arg223His(p.R223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233121
Start	27024120:27024120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292A>G
AA Mutation	p.Lys98Glu(p.K98E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233121
Start	27026318:27026318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233121
Start	27025695:27025695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113977877
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAPRE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233121
Start	27024235:27024235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761152460
CDS Mutation	c.407C>T
AA Mutation	p.Ala136Val(p.A136V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript