Mutation

Primary Site >> Stomach Cancer

Gene >> UPF1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18846063:18846063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315C>G
AA Mutation	p.Phe105Leu(p.F105L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18856979:18856979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1960G>A
AA Mutation	p.Glu654Lys(p.E654K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18852249:18852249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925C>G
AA Mutation	p.Leu309Val(p.L309V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18857007:18857007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1988T>C
AA Mutation	p.Leu663Pro(p.L663P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18853306:18853306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1145C>T
AA Mutation	p.Ala382Val(p.A382V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18860339:18860339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2234G>C
AA Mutation	p.Gly745Ala(p.G745A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18850124:18850124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511C>T
AA Mutation	p.His171Tyr(p.H171Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18856880:18856880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1861G>A
AA Mutation	p.Ala621Thr(p.A621T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18857431:18857431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2113C>T
AA Mutation	p.Arg705Trp(p.R705W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18854899:18854899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319C>T
AA Mutation	p.Thr440Met(p.T440M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18855990:18855990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1643C>T
AA Mutation	p.Thr548Met(p.T548M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18864177:18864177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2816G>A
AA Mutation	p.Arg939His(p.R939H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18854686:18854686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18855228:18855228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18856960:18856960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140516243
CDS Mutation	c.1941C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18865580:18865580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3072C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18866136:18866136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776035891
CDS Mutation	c.3363C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18854638:18854638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144265702
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18846084:18846084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000599848
Start	18856005:18856012(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1664_1671delTCTGCGCC
AA Mutation	p.Leu555GlnfsTer4(p.L555Qfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000599848
Start	18864250:18864250(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2890+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000599848
Start	18850848:18850848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790A>T
AA Mutation	p.Lys264Ter(p.K264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript