Mutation

Primary Site >> Stomach Cancer

Gene >> PPP1R3A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113878011:113878011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3081A>C
AA Mutation	p.Glu1027Asp(p.E1027D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879631:113879631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461A>C
AA Mutation	p.Arg487Ser(p.R487S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879690:113879690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402A>G
AA Mutation	p.Lys468Glu(p.K468E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879381:113879381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765161960
CDS Mutation	c.1711G>A
AA Mutation	p.Ala571Thr(p.A571T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879611:113879611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17847377
CDS Mutation	c.1481C>T
AA Mutation	p.Ser494Leu(p.S494L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113882157:113882157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.848A>G
AA Mutation	p.Tyr283Cys(p.Y283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879869:113879869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1223C>T
AA Mutation	p.Thr408Ile(p.T408I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879345:113879345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1747C>T
AA Mutation	p.His583Tyr(p.H583Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113878165:113878165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2927T>C
AA Mutation	p.Val976Ala(p.V976A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879388:113879388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1704A>C
AA Mutation	p.Glu568Asp(p.E568D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879746:113879746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346G>A
AA Mutation	p.Gly449Asp(p.G449D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113918302:113918302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695A>G
AA Mutation	p.Gln232Arg(p.Q232R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113918849:113918849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148G>A
AA Mutation	p.Glu50Lys(p.E50K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879835:113879835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257G>T
AA Mutation	p.Leu419Phe(p.L419F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113918946:113918946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51A>C
AA Mutation	p.Glu17Asp(p.E17D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113878411:113878411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140543337
CDS Mutation	c.2681C>T
AA Mutation	p.Ser894Leu(p.S894L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113882314:113882314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.789A>C
AA Mutation	p.Glu263Asp(p.E263D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113878487:113878487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2605T>G
AA Mutation	p.Leu869Val(p.L869V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113918587:113918587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410T>C
AA Mutation	p.Leu137Pro(p.L137P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879689:113879689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1403A>C
AA Mutation	p.Lys468Thr(p.K468T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113918570:113918570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427A>G
AA Mutation	p.Lys143Glu(p.K143E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113878313:113878313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373483153
CDS Mutation	c.2779A>G
AA Mutation	p.Thr927Ala(p.T927A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113918846:113918846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151G>C
AA Mutation	p.Asp51His(p.D51H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113878808:113878808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2284A>C
AA Mutation	p.Ser762Arg(p.S762R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113879942:113879942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533705714
CDS Mutation	c.1150G>A
AA Mutation	p.Val384Ile(p.V384I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113918486:113918486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>C
AA Mutation	p.Asp171His(p.D171H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113918236:113918236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764900818
CDS Mutation	c.761G>A
AA Mutation	p.Gly254Asp(p.G254D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000284601
Start	113918495:113918495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502A>T
AA Mutation	p.Thr168Ser(p.T168S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284601
Start	113918709:113918709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111896635
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284601
Start	113878800:113878800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2292G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284601
Start	113879883:113879883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1209A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284601
Start	113879931:113879931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284601
Start	113879424:113879424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1668A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284601
Start	113878545:113878545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142590001
CDS Mutation	c.2547A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284601
Start	113879376:113879376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1716C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284601
Start	113879223:113879223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1869A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000284601
Start	113878847:113878847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2245A>T
AA Mutation	p.Lys749Ter(p.K749*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000284601
Start	113878124:113878124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2968G>T
AA Mutation	p.Glu990Ter(p.E990*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000284601
Start	113878553:113878553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2539G>T
AA Mutation	p.Glu847Ter(p.E847*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	stop_gained
Transcription ID	ENST00000284601
Start	113879319:113879319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1773G>A
AA Mutation	p.Trp591Ter(p.W591*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284601
Start	113878342:113878343(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2749dupT
AA Mutation	p.Ser917PhefsTer6(p.S917Ffs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript