Mutation

Primary Site >> Stomach Cancer

Gene >> POLD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50407008:50407008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1520G>A
AA Mutation	p.Arg507His(p.R507H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50402315:50402315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700G>A
AA Mutation	p.Ala234Thr(p.A234T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50402702:50402702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201010746
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Cys(p.R311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50408846:50408846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1837G>T
AA Mutation	p.Ala613Ser(p.A613S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50407061:50407061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201804732
CDS Mutation	c.1573C>T
AA Mutation	p.Arg525Trp(p.R525W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50402717:50402717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946G>A
AA Mutation	p.Asp316Asn(p.D316N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000440232
Start	50403053:50403053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971G>T
AA Mutation	p.Gly324Val(p.G324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50413453:50413453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2182A>C
AA Mutation	p.Ile728Leu(p.I728L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50401838:50401838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377G>A
AA Mutation	p.Arg126His(p.R126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50407402:50407402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746649739
CDS Mutation	c.1762G>A
AA Mutation	p.Glu588Lys(p.E588K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000440232
Start	50414840:50414840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2414G>A
AA Mutation	p.Ser805Asn(p.S805N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440232
Start	50409600:50409600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2088C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440232
Start	50402347:50402347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778836055
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440232
Start	50413753:50413753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2262T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440232
Start	50402305:50402305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000440232
Start	50413855:50413855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2364G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440232
Start	50401804:50401804(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.347delC
AA Mutation	p.Pro116HisfsTer53(p.P116Hfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000440232
Start	50402066:50402067(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.537dupG
AA Mutation	p.Arg180GlufsTer72(p.R180Efs*72)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000440232
Start	50413741:50413741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2251-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript