Mutation

Primary Site >> Stomach Cancer

Gene >> FZD4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000531380
Start	86951483:86951483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273A>G
AA Mutation	p.Thr425Ala(p.T425A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000531380
Start	86951944:86951944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812T>C
AA Mutation	p.Val271Ala(p.V271A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000531380
Start	86952118:86952118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374499509
CDS Mutation	c.638G>A
AA Mutation	p.Arg213His(p.R213H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000531380
Start	86951332:86951332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1424C>T
AA Mutation	p.Ala475Val(p.A475V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000531380
Start	86951300:86951300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1456T>G
AA Mutation	p.Leu486Val(p.L486V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000531380
Start	86952257:86952257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499G>T
AA Mutation	p.Val167Leu(p.V167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000531380
Start	86952451:86952451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305A>T
AA Mutation	p.Tyr102Phe(p.Y102F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531380
Start	86952027:86952027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560649393
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531380
Start	86951691:86951691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751317286
CDS Mutation	c.1065C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531380
Start	86952000:86952000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000531380
Start	86951161:86951161(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1595delG
AA Mutation	p.Gly532AlafsTer46(p.G532Afs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000531380
Start	86951770:86951770(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.986delT
AA Mutation	p.Leu329TrpfsTer29(p.L329Wfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript