Colon Cancer: Gene >> HDAC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000519065
Start	113943500:113943500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1229C>T
AA Mutation	p.Ala410Val(p.A410V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000519065
Start	113946115:113946115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875T>G
AA Mutation	p.Phe292Cys(p.F292C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000519065
Start	113959917:113959917(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.154delA
AA Mutation	p.Met52TrpfsTer14(p.M52Wfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000519065
Start	113943354:113943354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1375delA
AA Mutation	p.Thr459GlnfsTer47(p.T459Qfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000519065
Start	113943504:113943504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267600769
CDS Mutation	c.1225C>T
AA Mutation	p.Arg409Ter(p.R409*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000519065
Start	113956131:113956131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379C>T
AA Mutation	p.Arg127Ter(p.R127*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000519065
Start	113956695:113956695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HDAC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000519065
Start	113945452:113945452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001A>G
AA Mutation	p.Tyr334Cys(p.Y334C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519065
Start	113956629:113956629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373430125
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000519065
Start	113953323:113953323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593C>A
AA Mutation	p.Ser198Ter(p.S198*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript