Mutation

Primary Site >> Stomach Cancer

Gene >> FZD8

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35639751:35639751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768002036
CDS Mutation	c.1679G>A
AA Mutation	p.Arg560His(p.R560H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35639899:35639899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1531C>T
AA Mutation	p.Arg511Cys(p.R511C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35640159:35640159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1271C>T
AA Mutation	p.Ala424Val(p.A424V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35640628:35640628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802T>C
AA Mutation	p.Phe268Leu(p.F268L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35639785:35639785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1645G>A
AA Mutation	p.Ala549Thr(p.A549T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35640249:35640249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1181C>T
AA Mutation	p.Ala394Val(p.A394V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35640040:35640040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1390G>A
AA Mutation	p.Gly464Ser(p.G464S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35640183:35640183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1247T>A
AA Mutation	p.Ile416Asn(p.I416N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35641273:35641273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157A>G
AA Mutation	p.Met53Val(p.M53V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35639574:35639574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1856G>A
AA Mutation	p.Arg619His(p.R619H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35639757:35639757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673G>A
AA Mutation	p.Arg558His(p.R558H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35641128:35641128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302A>C
AA Mutation	p.Lys101Thr(p.K101T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35641030:35641030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Cys(p.R134C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000374694
Start	35640442:35640442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Cys(p.R330C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35640176:35640176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35640458:35640458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35639678:35639678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372059031
CDS Mutation	c.1752C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35639960:35639960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1470C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35640545:35640545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35640248:35640248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374694
Start	35639978:35639978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374694
Start	35641302:35641309(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.121_128delCCGCTGTG
AA Mutation	p.Pro41Ter(p.P41*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000374694
Start	35640092:35640092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338G>A
AA Mutation	p.Trp446Ter(p.W446*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript