Mutation

Primary Site >> Stomach Cancer

Gene >> SIN3A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360439
Start	75400062:75400062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832G>A
AA Mutation	p.Arg611His(p.R611H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360439
Start	75372014:75372014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374431322
CDS Mutation	c.3787C>T
AA Mutation	p.Arg1263Cys(p.R1263C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360439
Start	75396460:75396460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1891C>T
AA Mutation	p.Arg631Trp(p.R631W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360439
Start	75372168:75372168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3633G>T
AA Mutation	p.Gln1211His(p.Q1211H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360439
Start	75413014:75413014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505T>C
AA Mutation	p.Ser169Pro(p.S169P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360439
Start	75414301:75414301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377C>T
AA Mutation	p.Ala126Val(p.A126V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360439
Start	75410266:75410266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1029G>T
AA Mutation	p.Lys343Asn(p.K343N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360439
Start	75396415:75396415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1936G>A
AA Mutation	p.Glu646Lys(p.E646K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360439
Start	75400048:75400048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1846C>T
AA Mutation	p.Arg616Cys(p.R616C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360439
Start	75384408:75384408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3051T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360439
Start	75392705:75392705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2388C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360439
Start	75411633:75411633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769881227
CDS Mutation	c.867G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360439
Start	75372078:75372078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3723C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360439
Start	75401908:75401908(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1470delT
AA Mutation	p.Phe490LeufsTer5(p.F490Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360439
Start	75411680:75411680(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.820delT
AA Mutation	p.Ser274ProfsTer13(p.S274Pfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360439
Start	75392408:75392408(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2685delT
AA Mutation	p.Phe895LeufsTer10(p.F895Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000360439
Start	75372143:75372143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3658G>T
AA Mutation	p.Glu1220Ter(p.E1220*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000360439
Start	75394805:75394805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2152C>T
AA Mutation	p.Arg718Ter(p.R718*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000360439
Start	75394838:75394838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2119C>T
AA Mutation	p.Arg707Ter(p.R707*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000360439
Start	75384404:75384404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3055C>T
AA Mutation	p.Gln1019Ter(p.Q1019*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000360439
Start	75396343:75396343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2008C>T
AA Mutation	p.Gln670Ter(p.Q670*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360439
Start	75407060:75407061(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1401dupT
AA Mutation	p.Asp468Ter(p.D468*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript