Mutation

Primary Site >> Stomach Cancer

Gene >> HDAC5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44078650:44078650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533094138
CDS Mutation	c.3179G>A
AA Mutation	p.Cys1060Tyr(p.C1060Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44093632:44093632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.297G>T
AA Mutation	p.Gln99His(p.Q99H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44091426:44091426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1231G>A
AA Mutation	p.Gly411Ser(p.G411S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44088568:44088568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775955049
CDS Mutation	c.1418C>T
AA Mutation	p.Thr473Met(p.T473M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44092401:44092401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899T>C
AA Mutation	p.Ile300Thr(p.I300T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44084671:44084671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2189T>A
AA Mutation	p.Ile730Asn(p.I730N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44093715:44093715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746035403
CDS Mutation	c.214C>T
AA Mutation	p.Arg72Trp(p.R72W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44083838:44083838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2322G>T
AA Mutation	p.Lys774Asn(p.K774N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44083851:44083851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2309C>A
AA Mutation	p.Pro770His(p.P770H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44085029:44085029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2177A>C
AA Mutation	p.Lys726Thr(p.K726T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44087646:44087646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1650G>T
AA Mutation	p.Glu550Asp(p.E550D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000586802
Start	44091369:44091369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370605385
CDS Mutation	c.1288G>A
AA Mutation	p.Val430Met(p.V430M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000586802
Start	44092794:44092794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654T>C
Mutation Classification	Silent
Feature Type	Transcript

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

ID	15
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000586802
Start	44082670:44082670(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2522delG
AA Mutation	p.Gly841AspfsTer8(p.G841Dfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

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