Mutation

Primary Site >> Stomach Cancer

Gene >> PHLPP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62979229:62979229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4952A>G
AA Mutation	p.Tyr1651Cys(p.Y1651C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62975432:62975432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3791C>T
AA Mutation	p.Ala1264Val(p.A1264V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62978773:62978773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201439333
CDS Mutation	c.4496C>T
AA Mutation	p.Pro1499Leu(p.P1499L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62895860:62895860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2293C>A
AA Mutation	p.Leu765Met(p.L765M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62903034:62903034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2515C>G
AA Mutation	p.Arg839Gly(p.R839G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62963412:62963412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3500C>T
AA Mutation	p.Ala1167Val(p.A1167V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62919982:62919982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2828G>A
AA Mutation	p.Arg943Gln(p.R943Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62978473:62978473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4196C>T
AA Mutation	p.Ala1399Val(p.A1399V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262719
Start	62972689:62972689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3736A>G
AA Mutation	p.Thr1246Ala(p.T1246A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262719
Start	62972583:62972583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367669597
CDS Mutation	c.3630C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262719
Start	62941844:62941844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3087G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262719
Start	62838831:62838831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1821T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262719
Start	62972653:62972654(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3706dupA
AA Mutation	p.Thr1236AsnfsTer38(p.T1236Nfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262719
Start	62896006:62896007(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2440_2443dupCTAA
AA Mutation	p.Arg815ThrfsTer7(p.R815Tfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript