Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HDAC9

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000432645
Start 18496324:18496324(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.22G>T
AA Mutation p.Val8Leu(p.V8L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18585477:18585477(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.219G>T
AA Mutation p.Glu73Asp(p.E73D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18629433:18629433(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.739G>T
AA Mutation p.Asp247Tyr(p.D247Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18762226:18762226(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2104T>C
AA Mutation p.Tyr702His(p.Y702H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18727620:18727620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1763G>A
AA Mutation p.Arg588His(p.R588H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18644719:18644719(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.952C>A
AA Mutation p.Leu318Met(p.L318M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18835557:18835557(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2548T>G
AA Mutation p.Phe850Val(p.F850V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18749116:18749116(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2012C>T
AA Mutation p.Thr671Ile(p.T671I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18666370:18666370(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1616T>C
AA Mutation p.Leu539Pro(p.L539P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18835540:18835540(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2531G>A
AA Mutation p.Arg844His(p.R844H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18591587:18591587(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.478A>C
AA Mutation p.Thr160Pro(p.T160P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18585513:18585513(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.255G>T
AA Mutation p.Glu85Asp(p.E85D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18585380:18585380(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.122T>A
AA Mutation p.Val41Asp(p.V41D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18874588:18874588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2786C>T
AA Mutation p.Thr929Met(p.T929M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000441542
Start 18975873:18975873(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs531869853
CDS Mutation c.3090G>T
AA Mutation p.Leu1030Phe(p.L1030F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18793357:18793357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2218A>G
AA Mutation p.Thr740Ala(p.T740A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18647822:18647822(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367766754
CDS Mutation c.1064C>T
AA Mutation p.Thr355Met(p.T355M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18585383:18585383(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763335887
CDS Mutation c.125G>A
AA Mutation p.Arg42His(p.R42H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18594004:18594004(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.630G>T
AA Mutation p.Lys210Asn(p.K210N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18835539:18835539(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2530C>T
AA Mutation p.Arg844Cys(p.R844C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18666473:18666473(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1719A>T
AA Mutation p.Gln573His(p.Q573H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18591584:18591584(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.475G>A
AA Mutation p.Asp159Asn(p.D159N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000432645
Start 18591642:18591642(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.533C>T
AA Mutation p.Thr178Met(p.T178M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18749083:18749083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777828245
CDS Mutation c.1979G>A
AA Mutation p.Arg660Gln(p.R660Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18727722:18727722(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1865C>A
AA Mutation p.Ala622Glu(p.A622E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18585471:18585471(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.213G>T
AA Mutation p.Gln71His(p.Q71H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18585473:18585473(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.215A>T
AA Mutation p.His72Leu(p.H72L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000441542
Start 18975921:18975921(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3138T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18585291:18585291(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374974366
CDS Mutation c.33G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18954184:18954184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2967G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18727597:18727597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1740G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18727609:18727609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1752G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18935858:18935858(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371134945
CDS Mutation c.2844G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18874556:18874556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2754C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18935876:18935876(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2862A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18585471:18585471(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs187797966
CDS Mutation c.213G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18727639:18727639(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1782G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18647790:18647790(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765691093
CDS Mutation c.1032G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000432645
Start 18666406:18666412(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1657_1663delGACAGTG
AA Mutation p.Asp553MetfsTer46(p.D553Mfs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 40
Mutation Consequence stop_gained
Transcription ID ENST00000432645
Start 18590441:18590441(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.361G>T
AA Mutation p.Glu121Ter(p.E121*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence stop_gained
Transcription ID ENST00000432645
Start 18835494:18835494(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2485C>T
AA Mutation p.Gln829Ter(p.Q829*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence stop_gained
Transcription ID ENST00000432645
Start 18647974:18647974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1216C>T
AA Mutation p.Arg406Ter(p.R406*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000432645
Start 18590344:18590344(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.265-1G>T
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 44
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000432645
Start 18829160:18829160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2314-1G>T
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 45
Mutation Consequence splice_donor_variant
Transcription ID ENST00000441542
Start 18975954:18975954(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3170+1G>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> HDAC9

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18647789:18647789(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1031C>T
AA Mutation p.Ser344Leu(p.S344L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18935914:18935914(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2900C>A
AA Mutation p.Ala967Asp(p.A967D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18585364:18585364(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376682964
CDS Mutation c.106G>A
AA Mutation p.Val36Met(p.V36M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18762163:18762163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2041C>A
AA Mutation p.Gln681Lys(p.Q681K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18874590:18874590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2788G>T
AA Mutation p.Ala930Ser(p.A930S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18727712:18727712(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1855C>T
AA Mutation p.Pro619Ser(p.P619S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18954211:18954211(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2994G>T
AA Mutation p.Gln998His(p.Q998H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18647790:18647790(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765691093
CDS Mutation c.1032G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18727597:18727597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1740G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18591613:18591613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757411806
CDS Mutation c.504C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18594010:18594010(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.636T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18647877:18647877(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771090434
CDS Mutation c.1119G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000432645
Start 18762187:18762187(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2065G>T
AA Mutation p.Glu689Ter(p.E689*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000432645
Start 18591533:18591533(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.424G>T
AA Mutation p.Glu142Ter(p.E142*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000432645
Start 18829160:18829160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2314-1G>T
Mutation Classification Splice_Site
Feature Type Transcript