Colon Cancer: Gene >> HDAC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44091359:44091359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1298A>G
AA Mutation	p.Glu433Gly(p.E433G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44086679:44086679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1943T>C
AA Mutation	p.Leu648Pro(p.L648P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44087458:44087458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1838C>T
AA Mutation	p.Ala613Val(p.A613V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44088436:44088436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1550A>G
AA Mutation	p.His517Arg(p.H517R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44092281:44092281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369028803
CDS Mutation	c.923C>T
AA Mutation	p.Ser308Leu(p.S308L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44082598:44082598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2594T>C
AA Mutation	p.Leu865Pro(p.L865P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44087574:44087574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1722G>T
AA Mutation	p.Glu574Asp(p.E574D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44078831:44078831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776063265
CDS Mutation	c.3127G>A
AA Mutation	p.Ala1043Thr(p.A1043T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44092760:44092760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775168585
CDS Mutation	c.688G>A
AA Mutation	p.Gly230Ser(p.G230S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44087425:44087425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1871C>A
AA Mutation	p.Ala624Asp(p.A624D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44085077:44085077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2129G>A
AA Mutation	p.Arg710Gln(p.R710Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586802
Start	44092280:44092280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750170598
CDS Mutation	c.924G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586802
Start	44080463:44080463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139019058
CDS Mutation	c.2763C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586802
Start	44085112:44085112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2094C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586802
Start	44078826:44078826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3132G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000586802
Start	44080433:44080433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2793delC
AA Mutation	p.Ile932LeufsTer14(p.I932Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000586802
Start	44087599:44087600(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1696dupG
AA Mutation	p.Glu566GlyfsTer15(p.E566Gfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000586802
Start	44080432:44080433(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs770174487
CDS Mutation	c.2793dupC
AA Mutation	p.Ile932HisfsTer24(p.I932Hfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HDAC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44078831:44078831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776063265
CDS Mutation	c.3127G>A
AA Mutation	p.Ala1043Thr(p.A1043T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript