Mutation

Primary Site >> Stomach Cancer

Gene >> HDAC4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239134558:239134558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772767638
CDS Mutation	c.1064C>T
AA Mutation	p.Thr355Met(p.T355M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239144597:239144597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746612197
CDS Mutation	c.851C>T
AA Mutation	p.Pro284Leu(p.P284L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239134422:239134422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115644432
CDS Mutation	c.1117G>A
AA Mutation	p.Ala373Thr(p.A373T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239053508:239053508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3167T>A
AA Mutation	p.Val1056Asp(p.V1056D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239087573:239087573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2415G>T
AA Mutation	p.Glu805Asp(p.E805D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239108160:239108160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1987C>G
AA Mutation	p.Leu663Val(p.L663V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239126656:239126656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770769407
CDS Mutation	c.1318G>A
AA Mutation	p.Ala440Thr(p.A440T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239102890:239102890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142554712
CDS Mutation	c.2104C>T
AA Mutation	p.Arg702Cys(p.R702C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239111687:239111687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1802G>A
AA Mutation	p.Arg601Gln(p.R601Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239190062:239190062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761550650
CDS Mutation	c.110C>T
AA Mutation	p.Ala37Val(p.A37V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000345617
Start	239095054:239095054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2221T>C
AA Mutation	p.Ser741Pro(p.S741P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239081104:239081104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2726C>T
AA Mutation	p.Ala909Val(p.A909V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239139767:239139767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745919731
CDS Mutation	c.895G>A
AA Mutation	p.Gly299Arg(p.G299R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
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

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239156685:239156685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549858743
CDS Mutation	c.700G>A
AA Mutation	p.Asp234Asn(p.D234N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239156702:239156702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683C>T
AA Mutation	p.Pro228Leu(p.P228L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239054805:239054805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3017A>G
AA Mutation	p.Gln1006Arg(p.Q1006R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239066781:239066781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760702458
CDS Mutation	c.2929G>A
AA Mutation	p.Asp977Asn(p.D977N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000345617
Start	239163816:239163816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754027484
CDS Mutation	c.598C>T
AA Mutation	p.Arg200Cys(p.R200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239082168:239082168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2571C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239134593:239134593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345617
Start	239053516:239053516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142279745
CDS Mutation	c.3159C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
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

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345617
Start	239111548:239111548(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1941delC
AA Mutation	p.Thr648ProfsTer14(p.T648Pfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345617
Start	239156703:239156712(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.673_682delTATAACCACC
AA Mutation	p.Tyr225ArgfsTer23(p.Y225Rfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345617
Start	239144603:239144603(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.845delA
AA Mutation	p.Lys282SerfsTer116(p.K282Sfs*116)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000345617
Start	239115076:239115076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1753G>T
AA Mutation	p.Glu585Ter(p.E585*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000345617
Start	239053459:239053459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3215+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript