Mutation

Primary Site >> Stomach Cancer

Gene >> PLG

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160752950:160752950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2322A>C
AA Mutation	p.Leu774Phe(p.L774F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160714892:160714892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646G>T
AA Mutation	p.Ala216Ser(p.A216S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160714829:160714829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583G>T
AA Mutation	p.Gly195Cys(p.G195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160718791:160718791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049C>T
AA Mutation	p.Pro350Leu(p.P350L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160739126:160739126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369196761
CDS Mutation	c.1936G>A
AA Mutation	p.Glu646Lys(p.E646K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160706449:160706449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92C>T
AA Mutation	p.Ala31Val(p.A31V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160716695:160716695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.719A>G
AA Mutation	p.Glu240Gly(p.E240G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160731124:160731124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574500945
CDS Mutation	c.1330G>A
AA Mutation	p.Val444Ile(p.V444I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000308192
Start	160713124:160713124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546A>C
AA Mutation	p.Glu182Asp(p.E182D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160738573:160738573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1838C>T
AA Mutation	p.Ser613Phe(p.S613F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160741367:160741367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2075T>C
AA Mutation	p.Val692Ala(p.V692A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160718437:160718437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931C>G
AA Mutation	p.Pro311Ala(p.P311A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000308192
Start	160752932:160752932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2304G>T
AA Mutation	p.Glu768Asp(p.E768D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308192
Start	160718382:160718382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753737813
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308192
Start	160736990:160736990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1785A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308192
Start	160722511:160722511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1200T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308192
Start	160731189:160731189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368155641
CDS Mutation	c.1395G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308192
Start	160736952:160736952(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1752delG
AA Mutation	p.Cys585ValfsTer27(p.C585Vfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308192
Start	160718418:160718419(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.919_920dupCA
AA Mutation	p.Asn308IlefsTer64(p.N308Ifs*64)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308192
Start	160711177:160711178(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.397dupC
AA Mutation	p.His133ProfsTer4(p.H133Pfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308192
Start	160714859:160714860(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.615dupA
AA Mutation	p.Cys206MetfsTer31(p.C206Mfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000308192
Start	160752262:160752262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2271+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000308192
Start	160731234:160731234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript