Mutation

Primary Site >> Stomach Cancer

Gene >> SCN9A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166199381:166199381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5258A>G
AA Mutation	p.Asn1753Ser(p.N1753S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166278153:166278153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375375336
CDS Mutation	c.2504G>A
AA Mutation	p.Arg835Gln(p.R835Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166284643:166284643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1784A>G
AA Mutation	p.Gln595Arg(p.Q595R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166288637:166288637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114C>T
AA Mutation	p.Arg372Cys(p.R372C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166199516:166199516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5123T>C
AA Mutation	p.Leu1708Pro(p.L1708P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166199454:166199454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5185G>T
AA Mutation	p.Asp1729Tyr(p.D1729Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166198873:166198873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5766A>C
AA Mutation	p.Arg1922Ser(p.R1922S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166199300:166199300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5339A>G
AA Mutation	p.Glu1780Gly(p.E1780G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166199724:166199724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4915A>G
AA Mutation	p.Met1639Val(p.M1639V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166198983:166198983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560168893
CDS Mutation	c.5656C>T
AA Mutation	p.Arg1886Trp(p.R1886W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166278225:166278225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2432T>A
AA Mutation	p.Phe811Tyr(p.F811Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166204189:166204189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4540A>T
AA Mutation	p.Asn1514Tyr(p.N1514Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166284634:166284634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201318927
CDS Mutation	c.1793G>A
AA Mutation	p.Arg598His(p.R598H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166284756:166284756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1671C>A
AA Mutation	p.Phe557Leu(p.F557L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166305831:166305831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557A>G
AA Mutation	p.Asp186Gly(p.D186G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166307049:166307049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284A>C
AA Mutation	p.Lys95Thr(p.K95T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166277095:166277095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2762T>A
AA Mutation	p.Phe921Tyr(p.F921Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166199036:166199036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5603T>G
AA Mutation	p.Met1868Arg(p.M1868R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166204141:166204141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577681720
CDS Mutation	c.4588G>A
AA Mutation	p.Val1530Ile(p.V1530I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166198961:166198961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5678C>T
AA Mutation	p.Ala1893Val(p.A1893V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166284589:166284589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200671761
CDS Mutation	c.1838C>T
AA Mutation	p.Pro613Leu(p.P613L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166305837:166305837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551T>G
AA Mutation	p.Leu184Arg(p.L184R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166198982:166198982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774488202
CDS Mutation	c.5657G>A
AA Mutation	p.Arg1886Gln(p.R1886Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166198707:166198707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5932G>C
AA Mutation	p.Asp1978His(p.D1978H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166233452:166233452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3812T>C
AA Mutation	p.Val1271Ala(p.V1271A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166284631:166284631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1796G>A
AA Mutation	p.Ser599Asn(p.S599N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166226688:166226688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4277A>G
AA Mutation	p.Lys1426Arg(p.K1426R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166311548:166311548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209T>C
AA Mutation	p.Met70Thr(p.M70T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166198679:166198679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5960A>C
AA Mutation	p.Lys1987Thr(p.K1987T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166277042:166277042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2815G>A
AA Mutation	p.Ala939Thr(p.A939T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166233395:166233395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368396027
CDS Mutation	c.3869G>A
AA Mutation	p.Arg1290Gln(p.R1290Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166311681:166311681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199933920
CDS Mutation	c.76C>T
AA Mutation	p.Arg26Cys(p.R26C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166277167:166277167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2690G>A
AA Mutation	p.Cys897Tyr(p.C897Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000303354
Start	166277236:166277236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201233619
CDS Mutation	c.2621C>T
AA Mutation	p.Ala874Val(p.A874V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303354
Start	166277271:166277271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2586A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303354
Start	166311718:166311718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303354
Start	166277208:166277208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200618289
CDS Mutation	c.2649C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303354
Start	166284693:166284693(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1734delT
AA Mutation	p.Phe578LeufsTer37(p.F578Lfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303354
Start	166288455:166288455(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1296delA
AA Mutation	p.Glu433SerfsTer36(p.E433Sfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303354
Start	166311737:166311737(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.20delC
AA Mutation	p.Pro7GlnfsTer83(p.P7Qfs*83)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303354
Start	166198849:166198849(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5790delA
AA Mutation	p.Asp1931IlefsTer31(p.D1931Ifs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303354
Start	166198675:166198675(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5964delA
AA Mutation	p.Lys1988AsnfsTer20(p.K1988Nfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	43
Mutation Consequence	stop_gained
Transcription ID	ENST00000303354
Start	166272521:166272521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3229C>T
AA Mutation	p.Gln1077Ter(p.Q1077*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303354
Start	166199481:166199482(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5157dupA
AA Mutation	p.Val1720SerfsTer8(p.V1720Sfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303354
Start	166288454:166288455(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1296dupA
AA Mutation	p.Glu433ArgfsTer6(p.E433Rfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript