Mutation

Primary Site >> Stomach Cancer

Gene >> FZD6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103325002:103325002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896G>T
AA Mutation	p.Trp299Leu(p.W299L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103300133:103300133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754581593
CDS Mutation	c.26C>T
AA Mutation	p.Thr9Met(p.T9M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103330002:103330002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1889G>T
AA Mutation	p.Gly630Val(p.G630V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103324645:103324645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539A>T
AA Mutation	p.Gln180Leu(p.Q180L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103331454:103331454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2066A>G
AA Mutation	p.His689Arg(p.H689R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103318657:103318657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245T>C
AA Mutation	p.Val82Ala(p.V82A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358755
Start	103300237:103300237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130A>G
AA Mutation	p.Asn44Asp(p.N44D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358755
Start	103300129:103300129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358755
Start	103324799:103324799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762687532
CDS Mutation	c.693G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358755
Start	103329922:103329922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201910779
CDS Mutation	c.1809C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358755
Start	103329733:103329733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1620A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358755
Start	103328375:103328375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763029375
CDS Mutation	c.1500C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358755
Start	103324976:103324976(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.875delT
AA Mutation	p.Phe292SerfsTer10(p.F292Sfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358755
Start	103324763:103324763(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.662delT
AA Mutation	p.Leu221Ter(p.L221*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358755
Start	103329933:103329933(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1824delC
AA Mutation	p.Arg609GlyfsTer2(p.R609Gfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358755
Start	103325329:103325329(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1227delA
AA Mutation	p.Lys409AsnfsTer2(p.K409Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358755
Start	103328391:103328391(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1521delT
AA Mutation	p.Phe507LeufsTer25(p.F507Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript