Mutation

Primary Site >> Stomach Cancer

Gene >> PLK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689996:23689996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1745A>G
AA Mutation	p.Tyr582Cys(p.Y582C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689567:23689567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751350031
CDS Mutation	c.1499G>A
AA Mutation	p.Arg500His(p.R500H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689575:23689575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1507G>T
AA Mutation	p.Asp503Tyr(p.D503Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23679216:23679216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284G>T
AA Mutation	p.Arg95Met(p.R95M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23683886:23683886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>A
AA Mutation	p.Ala278Asp(p.A278D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689566:23689566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498C>T
AA Mutation	p.Arg500Cys(p.R500C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689872:23689872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1621C>T
AA Mutation	p.Leu541Phe(p.L541F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689597:23689597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1529A>G
AA Mutation	p.Tyr510Cys(p.Y510C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23688721:23688721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1246G>A
AA Mutation	p.Asp416Asn(p.D416N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23680958:23680958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.622A>G
AA Mutation	p.Lys208Glu(p.K208E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23679068:23679068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.136G>A
AA Mutation	p.Asp46Asn(p.D46N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23684062:23684062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150139246
CDS Mutation	c.1009C>T
AA Mutation	p.Arg337Trp(p.R337W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000300093
Start	23689666:23689666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1598A>G
AA Mutation	p.Asn533Ser(p.N533S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300093
Start	23679142:23679142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300093
Start	23680939:23680939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757775507
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300093
Start	23689248:23689248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300093
Start	23679104:23679104(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.176delT
AA Mutation	p.Leu59TrpfsTer56(p.L59Wfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300093
Start	23689623:23689623(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1555delA
AA Mutation	p.Ser519AlafsTer28(p.S519Afs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000300093
Start	23680180:23680180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Ter(p.R169*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000300093
Start	23687522:23687522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Ter(p.R364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000300093
Start	23689636:23689656(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1572_1592delCCTCAGCAACGGCAGCGTGCA
AA Mutation	p.His524_Val530del(p.H524_V530del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript