Colon Cancer: Gene >> RASSF10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000529419
Start	13009782:13009782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206A>G
AA Mutation	p.Asn69Ser(p.N69S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000529419
Start	13010493:13010493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917C>T
AA Mutation	p.Ala306Val(p.A306V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000529419
Start	13010838:13010838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1262A>G
AA Mutation	p.Gln421Arg(p.Q421R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529419
Start	13011010:13011010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1434T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RASSF10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000529419
Start	13010778:13010778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1202G>T
AA Mutation	p.Gly401Val(p.G401V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript