Mutation

Primary Site >> Stomach Cancer

Gene >> FZD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266750:91266750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1870G>A
AA Mutation	p.Gly624Ser(p.G624S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266298:91266298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1418T>C
AA Mutation	p.Leu473Pro(p.L473P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266429:91266429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1549C>T
AA Mutation	p.Arg517Cys(p.R517C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266243:91266243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363C>T
AA Mutation	p.Pro455Ser(p.P455S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91265802:91265802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.922C>T
AA Mutation	p.Leu308Phe(p.L308F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266337:91266337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1457C>T
AA Mutation	p.Ala486Val(p.A486V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266742:91266742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1862T>A
AA Mutation	p.Ile621Asn(p.I621N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266303:91266303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423G>A
AA Mutation	p.Gly475Arg(p.G475R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266267:91266267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1387C>G
AA Mutation	p.Leu463Val(p.L463V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000287934
Start	91266577:91266577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697A>C
AA Mutation	p.Glu566Ala(p.E566A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91265156:91265156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91265600:91265600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91266359:91266359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1479G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91266380:91266380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200075522
CDS Mutation	c.1500T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287934
Start	91266716:91266716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1836C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287934
Start	91265669:91265669(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.794delG
AA Mutation	p.Gly265AlafsTer143(p.G265Afs*143)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000287934
Start	91266185:91266185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305G>A
AA Mutation	p.Trp435Ter(p.W435*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript