Mutation

Primary Site >> Stomach Cancer

Gene >> KCNH1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	210920038:210920038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064T>G
AA Mutation	p.Val355Gly(p.V355G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	210804052:210804052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577A>G
AA Mutation	p.Tyr526Cys(p.Y526C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000271751
Start	211133867:211133867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79G>A
AA Mutation	p.Asp27Asn(p.D27N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	211082793:211082793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545C>A
AA Mutation	p.Ser182Tyr(p.S182Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	211018958:211018958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857T>A
AA Mutation	p.Leu286His(p.L286H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	211018958:211018958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857T>C
AA Mutation	p.Leu286Pro(p.L286P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	210683319:210683319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2932T>C
AA Mutation	p.Ser978Pro(p.S978P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	210919674:210919674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1428G>T
AA Mutation	p.Glu476Asp(p.E476D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	211019075:211019075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771008535
CDS Mutation	c.740A>G
AA Mutation	p.Asn247Ser(p.N247S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	210797706:210797706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1717C>T
AA Mutation	p.Arg573Cys(p.R573C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	210683947:210683947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2304G>C
AA Mutation	p.Lys768Asn(p.K768N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	211018958:211018958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857T>G
AA Mutation	p.Leu286Arg(p.L286R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	211018796:211018796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019G>A
AA Mutation	p.Gly340Glu(p.G340E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	210919862:210919862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240C>T
AA Mutation	p.Arg414Cys(p.R414C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	210683462:210683462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2789G>A
AA Mutation	p.Arg930Lys(p.R930K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	211107354:211107354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.103G>T
AA Mutation	p.Ala35Ser(p.A35S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000271751
Start	210683555:210683555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2696G>A
AA Mutation	p.Ser899Asn(p.S899N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271751
Start	210797719:210797719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749409939
CDS Mutation	c.1704C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271751
Start	210683833:210683833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374844541
CDS Mutation	c.2418C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271751
Start	210797623:210797623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1800G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271751
Start	210684118:210684118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2133C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271751
Start	210683818:210683818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369345537
CDS Mutation	c.2433C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271751
Start	210683719:210683719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200699122
CDS Mutation	c.2532C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271751
Start	210804027:210804027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271751
Start	210919881:210919881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138866428
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271751
Start	210775402:210775402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2058C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271751
Start	210684066:210684066(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2185delC
AA Mutation	p.Leu729Ter(p.L729*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271751
Start	211018825:211018825(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.990delT
AA Mutation	p.Phe330LeufsTer24(p.F330Lfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271751
Start	210683771:210683771(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2480delG
AA Mutation	p.Gly827AlafsTer48(p.G827Afs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271751
Start	211019194:211019195(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.620dupC
AA Mutation	p.His208SerfsTer10(p.H208Sfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript