Mutation

Primary Site >> Stomach Cancer

Gene >> SULF1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69601802:69601802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765825581
CDS Mutation	c.1034G>A
AA Mutation	p.Arg345His(p.R345H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69629589:69629589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754254864
CDS Mutation	c.2194C>T
AA Mutation	p.Arg732Trp(p.R732W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69576007:69576007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210G>A
AA Mutation	p.Met70Ile(p.M70I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69624074:69624074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758690728
CDS Mutation	c.1727G>A
AA Mutation	p.Arg576His(p.R576H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260128
Start	69638856:69638856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143009161
CDS Mutation	c.2549T>C
AA Mutation	p.Val850Ala(p.V850A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69603224:69603224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094C>T
AA Mutation	p.Ala365Val(p.A365V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69589075:69589075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668C>T
AA Mutation	p.Ala223Val(p.A223V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69658530:69658530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2611G>T
AA Mutation	p.Gly871Cys(p.G871C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69627828:69627828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2004G>T
AA Mutation	p.Lys668Asn(p.K668N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69564072:69564072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>T
AA Mutation	p.Arg33Trp(p.R33W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69603298:69603298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168G>T
AA Mutation	p.Asp390Tyr(p.D390Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69600748:69600748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880G>A
AA Mutation	p.Glu294Lys(p.E294K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69603293:69603293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1163T>C
AA Mutation	p.Leu388Pro(p.L388P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69564088:69564088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748661181
CDS Mutation	c.113G>A
AA Mutation	p.Arg38Gln(p.R38Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69576069:69576069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272G>T
AA Mutation	p.Arg91Leu(p.R91L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69624036:69624036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1689A>C
AA Mutation	p.Glu563Asp(p.E563D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69586467:69586467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200127043
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Cys(p.R175C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69603309:69603309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1179G>T
AA Mutation	p.Lys393Asn(p.K393N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69576047:69576047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250A>G
AA Mutation	p.Thr84Ala(p.T84A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69621192:69621192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202168144
CDS Mutation	c.1535G>A
AA Mutation	p.Arg512His(p.R512H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000260128
Start	69564070:69564070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95G>A
AA Mutation	p.Gly32Glu(p.G32E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260128
Start	69621091:69621091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260128
Start	69588998:69588998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260128
Start	69624084:69624084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260128
Start	69586373:69586373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260128
Start	69628186:69628186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2058G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260128
Start	69621136:69621136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146435519
CDS Mutation	c.1479C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260128
Start	69601791:69601791(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773014665
CDS Mutation	c.1029delT
AA Mutation	p.Phe343LeufsTer7(p.F343Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260128
Start	69621127:69621173(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1471_1517delAACCTCTACGCTCGCGGCTTCCATGACAAAGACAAAGAGTGCAGTTG
AA Mutation	p.Asn491Ter(p.N491*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260128
Start	69576014:69576014(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747316268
CDS Mutation	c.223delG
AA Mutation	p.Ala75ProfsTer8(p.A75Pfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260128
Start	69586400:69586400(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.461delC
AA Mutation	p.Pro154LeufsTer9(p.P154Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260128
Start	69603625:69603626(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1219dupT
AA Mutation	p.Trp407LeufsTer3(p.W407Lfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	33
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000260128
Start	69629578:69629580(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2185_2187delGAG
AA Mutation	p.Glu729del(p.E729del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript