Mutation

Primary Site >> Stomach Cancer

Gene >> ZNF473

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50046293:50046293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1850G>A
AA Mutation	p.Arg617Lys(p.R617K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50046046:50046046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603A>T
AA Mutation	p.Ser535Cys(p.S535C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50046722:50046722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2279G>T
AA Mutation	p.Cys760Phe(p.C760F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50045057:50045057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.614G>A
AA Mutation	p.Gly205Glu(p.G205E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50044915:50044915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472C>T
AA Mutation	p.Pro158Ser(p.P158S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50039255:50039255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104C>T
AA Mutation	p.Ala35Val(p.A35V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50046275:50046275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832G>A
AA Mutation	p.Arg611Lys(p.R611K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50046860:50046860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2417G>T
AA Mutation	p.Arg806Ile(p.R806I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50046397:50046397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764328881
CDS Mutation	c.1954G>A
AA Mutation	p.Gly652Arg(p.G652R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50039203:50039203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52G>A
AA Mutation	p.Gly18Arg(p.G18R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50047006:50047006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2563T>C
AA Mutation	p.Ser855Pro(p.S855P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000270617
Start	50044736:50044736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293T>A
AA Mutation	p.Ile98Asn(p.I98N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270617
Start	50045139:50045139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270617
Start	50046054:50046054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199603967
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270617
Start	50045412:50045412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202040286
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270617
Start	50046003:50046003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376386436
CDS Mutation	c.1560C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270617
Start	50041815:50041815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270617
Start	50045388:50045388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270617
Start	50046762:50046762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2319T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270617
Start	50039241:50039241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749422474
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270617
Start	50045427:50045427(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.987delT
AA Mutation	p.Phe329LeufsTer30(p.F329Lfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000270617
Start	50045286:50045286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843G>A
AA Mutation	p.Trp281Ter(p.W281*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270617
Start	50046072:50046073(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1635dupT
AA Mutation	p.Val546CysfsTer18(p.V546Cfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript