Colon Cancer: Gene >> HDAC8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373573
Start	72495215:72495215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148688742
CDS Mutation	c.491G>A
AA Mutation	p.Arg164Gln(p.R164Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373573
Start	72464559:72464559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.910G>A
AA Mutation	p.Gly304Arg(p.G304R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373573
Start	72489012:72489012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658G>T
AA Mutation	p.Gly220Trp(p.G220W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373573
Start	72495200:72495200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506T>G
AA Mutation	p.Phe169Cys(p.F169C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000373573
Start	72572695:72572695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67G>T
AA Mutation	p.Glu23Ter(p.E23*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HDAC8

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373573
Start	72351836:72351836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008T>G
AA Mutation	p.Phe336Leu(p.F336L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000373573
Start	72491008:72491008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript