Mutation

Primary Site >> Stomach Cancer

Gene >> PHLPP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71690614:71690614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757343484
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Cys(p.R172C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71658804:71658804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1997A>T
AA Mutation	p.Lys666Ile(p.K666I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71649860:71649860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770864666
CDS Mutation	c.3002G>A
AA Mutation	p.Arg1001His(p.R1001H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71649245:71649245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3617G>A
AA Mutation	p.Arg1206Gln(p.R1206Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71681892:71681892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749G>A
AA Mutation	p.Arg250Gln(p.R250Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71714651:71714651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145A>G
AA Mutation	p.Thr49Ala(p.T49A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71650010:71650010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748202550
CDS Mutation	c.2852G>A
AA Mutation	p.Arg951Gln(p.R951Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71656649:71656649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2312C>A
AA Mutation	p.Pro771His(p.P771H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71650004:71650004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2858T>G
AA Mutation	p.Leu953Arg(p.L953R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71678839:71678839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184G>A
AA Mutation	p.Arg395Lys(p.R395K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71649352:71649352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3510C>G
AA Mutation	p.Asp1170Glu(p.D1170E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71649779:71649779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148247641
CDS Mutation	c.3083C>T
AA Mutation	p.Ala1028Val(p.A1028V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71655324:71655324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759756307
CDS Mutation	c.2501C>T
AA Mutation	p.Thr834Met(p.T834M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71656677:71656677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2284A>G
AA Mutation	p.Ile762Val(p.I762V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71655249:71655249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2576T>C
AA Mutation	p.Val859Ala(p.V859A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71681852:71681852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.789G>C
AA Mutation	p.Glu263Asp(p.E263D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000568954
Start	71678831:71678831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1192A>G
AA Mutation	p.Met398Val(p.M398V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71655293:71655293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2532G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71667306:71667306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1656A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71649322:71649322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148712567
CDS Mutation	c.3540G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71681858:71681858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773235144
CDS Mutation	c.783C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71681870:71681870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746959350
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71678763:71678763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1260G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000568954
Start	71650018:71650018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2844C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000568954
Start	71702646:71702646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370G>T
AA Mutation	p.Glu124Ter(p.E124*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000568954
Start	71702712:71702712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304C>T
AA Mutation	p.Arg102Ter(p.R102*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript