Colon Cancer: Gene >> HDAC10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216271
Start	50246896:50246896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1493G>A
AA Mutation	p.Gly498Asp(p.G498D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216271
Start	50249416:50249416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.602G>A
AA Mutation	p.Arg201His(p.R201H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216271
Start	50250447:50250447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271G>A
AA Mutation	p.Asp91Asn(p.D91N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216271
Start	50246925:50246925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216271
Start	50249871:50249871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769079660
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HDAC10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216271
Start	50248688:50248688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202169873
CDS Mutation	c.880G>A
AA Mutation	p.Gly294Ser(p.G294S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript