Mutation

Primary Site >> Stomach Cancer

Gene >> ATP4A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35559969:35559969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892G>A
AA Mutation	p.Glu298Lys(p.E298K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35555330:35555330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145835787
CDS Mutation	c.2162C>T
AA Mutation	p.Ala721Val(p.A721V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35554978:35554978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778443222
CDS Mutation	c.2425G>A
AA Mutation	p.Val809Met(p.V809M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35559933:35559933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928G>A
AA Mutation	p.Ala310Thr(p.A310T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262623
Start	35559190:35559190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1058T>G
AA Mutation	p.Val353Gly(p.V353G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35562602:35562602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253C>T
AA Mutation	p.Arg85Trp(p.R85W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35550894:35550894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146641851
CDS Mutation	c.3019G>A
AA Mutation	p.Gly1007Ser(p.G1007S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35560017:35560017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844G>A
AA Mutation	p.Ala282Thr(p.A282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35558435:35558435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1427G>A
AA Mutation	p.Gly476Asp(p.G476D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35556962:35556962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561974216
CDS Mutation	c.1820G>A
AA Mutation	p.Arg607Gln(p.R607Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35554983:35554983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2420T>C
AA Mutation	p.Val807Ala(p.V807A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35555537:35555537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2060C>T
AA Mutation	p.Ser687Leu(p.S687L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35562580:35562580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275G>A
AA Mutation	p.Arg92Gln(p.R92Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35559127:35559127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121C>T
AA Mutation	p.Ala374Val(p.A374V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35551477:35551477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2855G>A
AA Mutation	p.Arg952His(p.R952H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35555710:35555710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767990060
CDS Mutation	c.1972C>T
AA Mutation	p.Arg658Cys(p.R658C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35555679:35555679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145767701
CDS Mutation	c.2003G>A
AA Mutation	p.Arg668His(p.R668H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35560507:35560507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376213037
CDS Mutation	c.643C>T
AA Mutation	p.Arg215Cys(p.R215C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35555555:35555555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2042T>C
AA Mutation	p.Leu681Pro(p.L681P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35557025:35557025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757C>T
AA Mutation	p.Ala586Val(p.A586V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35555319:35555319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767066130
CDS Mutation	c.2173G>A
AA Mutation	p.Val725Ile(p.V725I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35556935:35556935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1847A>G
AA Mutation	p.Lys616Arg(p.K616R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000262623
Start	35560007:35560007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375031967
CDS Mutation	c.854C>T
AA Mutation	p.Ala285Val(p.A285V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35562594:35562594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35560430:35560430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.720C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35563257:35563257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35559180:35559180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35554985:35554985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541790101
CDS Mutation	c.2418C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35560598:35560598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149907700
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35555203:35555203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2289T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35555254:35555254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2238C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35555476:35555476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2121G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35557024:35557024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1758C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35553106:35553106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757756460
CDS Mutation	c.2682C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35559090:35559090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262623
Start	35560039:35560039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262623
Start	35560056:35560056(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.805delG
AA Mutation	p.Val269TrpfsTer2(p.V269Wfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262623
Start	35553035:35553035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2751+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript