Colon Cancer: Gene >> HDAC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239134630:239134630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992A>G
AA Mutation	p.His331Arg(p.H331R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239139779:239139779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883G>A
AA Mutation	p.Ala295Thr(p.A295T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239163898:239163898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516G>C
AA Mutation	p.Lys172Asn(p.K172N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239054782:239054782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3040G>T
AA Mutation	p.Val1014Phe(p.V1014F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239111568:239111568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375565547
CDS Mutation	c.1921G>A
AA Mutation	p.Val641Met(p.V641M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239115088:239115088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771862462
CDS Mutation	c.1741C>T
AA Mutation	p.Arg581Cys(p.R581C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239236617:239236617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70C>T
AA Mutation	p.Arg24Cys(p.R24C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239144640:239144640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371367857
CDS Mutation	c.808C>T
AA Mutation	p.Arg270Cys(p.R270C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239163824:239163824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590G>A
AA Mutation	p.Ser197Asn(p.S197N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239190017:239190017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777568201
CDS Mutation	c.155G>A
AA Mutation	p.Arg52His(p.R52H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239111621:239111621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1868G>A
AA Mutation	p.Gly623Asp(p.G623D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239115175:239115175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373617636
CDS Mutation	c.1654G>A
AA Mutation	p.Ala552Thr(p.A552T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239139764:239139764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898C>T
AA Mutation	p.Pro300Ser(p.P300S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239189860:239189860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs6740794
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239163823:239163823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541806713
CDS Mutation	c.591C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239236660:239236660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239139687:239139687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345617
Start	239081127:239081127(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2703delC
AA Mutation	p.Met902TrpfsTer55(p.M902Wfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345617
Start	239144646:239144646(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.802delC
AA Mutation	p.Leu268CysfsTer13(p.L268Cfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345617
Start	239134372:239134372(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1167delC
AA Mutation	p.Gly390AlafsTer8(p.G390Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000345617
Start	239102860:239102860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2134C>T
AA Mutation	p.Gln712Ter(p.Q712*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000345617
Start	239189865:239189865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>T
AA Mutation	p.Gln103Ter(p.Q103*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000345617
Start	239054834:239054834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2989-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HDAC4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239053510:239053510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114003127
CDS Mutation	c.3165G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239163856:239163856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.558G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239102819:239102819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149067286
CDS Mutation	c.2175G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239139780:239139780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345617
Start	239081127:239081127(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2703delC
AA Mutation	p.Met902TrpfsTer55(p.M902Wfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript