Mutation

Primary Site >> Stomach Cancer

Gene >> RNF43

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58357510:58357510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2266C>T
AA Mutation	p.Pro756Ser(p.P756S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58415446:58415446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.132G>T
AA Mutation	p.Gln44His(p.Q44H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58358613:58358613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163A>G
AA Mutation	p.His388Arg(p.H388R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58371030:58371030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256C>T
AA Mutation	p.His86Tyr(p.H86Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000407977
Start	58362546:58362546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685C>T
AA Mutation	p.Pro229Ser(p.P229S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58358229:58358229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547A>G
AA Mutation	p.Asp516Gly(p.D516G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58360154:58360154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947T>C
AA Mutation	p.Ile316Thr(p.I316T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58371029:58371029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257A>G
AA Mutation	p.His86Arg(p.H86R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58362575:58362575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377765604
CDS Mutation	c.656G>A
AA Mutation	p.Arg219His(p.R219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000407977
Start	58362576:58362576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373068965
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Cys(p.R219C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407977
Start	58358348:58358348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1428T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407977
Start	58362547:58362547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58357800:58357800(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781215815
CDS Mutation	c.1976delG
AA Mutation	p.Gly659ValfsTer41(p.G659Vfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58363337:58363359(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.498_520delTAATGACGCTGAGAAGCTGATGG
AA Mutation	p.Asn167ValfsTer13(p.N167Vfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58360170:58360170(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.931delC
AA Mutation	p.Leu311SerfsTer108(p.L311Sfs*108)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58358489:58358489(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1287delT
AA Mutation	p.Ala430LeufsTer72(p.A430Lfs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58357770:58357792(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1984_2006delGAGCCCACCCCTGGCTCTCGGCC
AA Mutation	p.Glu662ProfsTer77(p.E662Pfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58358405:58358405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1371C>A
AA Mutation	p.Tyr457Ter(p.Y457*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58360872:58360872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760C>T
AA Mutation	p.Gln254Ter(p.Q254*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58363380:58363380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477G>A
AA Mutation	p.Trp159Ter(p.W159*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58360803:58360803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>T
AA Mutation	p.Glu277Ter(p.E277*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58358575:58358575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201G>T
AA Mutation	p.Glu401Ter(p.E401*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58415460:58415460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.118A>T
AA Mutation	p.Arg40Ter(p.R40*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000407977
Start	58358788:58358788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Ter(p.R330*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58358229:58358230(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1546dupG
AA Mutation	p.Asp516GlyfsTer10(p.D516Gfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58358417:58358418(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1357_1358dupGA
AA Mutation	p.Arg454AsnfsTer49(p.R454Nfs*49)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58360169:58360170(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.931dupC
AA Mutation	p.Leu311ProfsTer132(p.L311Pfs*132)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407977
Start	58415436:58415437(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.141dupT
AA Mutation	p.Ile48TyrfsTer27(p.I48Yfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	29
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000407977
Start	58357994:58357996(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1780_1782delCCT
AA Mutation	p.Pro594del(p.P594del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript