Mutation

Primary Site >> Stomach Cancer

Gene >> HDAC9

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18727697:18727697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749459197
CDS Mutation	c.1840G>A
AA Mutation	p.Ala614Thr(p.A614T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18648568:18648568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343G>A
AA Mutation	p.Arg448Gln(p.R448Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18935892:18935892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2878G>T
AA Mutation	p.Ala960Ser(p.A960S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18591583:18591583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474A>C
AA Mutation	p.Lys158Asn(p.K158N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18634671:18634671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832C>A
AA Mutation	p.Pro278Thr(p.P278T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18666333:18666333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579A>T
AA Mutation	p.Thr527Ser(p.T527S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18666334:18666334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1580C>A
AA Mutation	p.Thr527Asn(p.T527N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18749047:18749047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1943G>T
AA Mutation	p.Cys648Phe(p.C648F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18727731:18727731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1874G>A
AA Mutation	p.Arg625His(p.R625H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18835534:18835534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2525T>G
AA Mutation	p.Leu842Arg(p.L842R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000432645
Start	18591614:18591614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369824636
CDS Mutation	c.505G>A
AA Mutation	p.Val169Met(p.V169M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
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

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432645
Start	18629432:18629432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432645
Start	18648578:18648578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432645
Start	18648543:18648543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432645
Start	18935825:18935825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760139178
CDS Mutation	c.2811G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000441542
Start	18975891:18975891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3108C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432645
Start	18590377:18590377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432645
Start	18835484:18835484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374625281
CDS Mutation	c.2475C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432645
Start	18666308:18666308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432645
Start	18590467:18590467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000432645
Start	18835488:18835492(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2479_2483delACCCA
AA Mutation	p.Thr827AlafsTer6(p.T827Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000432645
Start	18585469:18585469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211C>T
AA Mutation	p.Gln71Ter(p.Q71*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript