Mutation

Primary Site >> Stomach Cancer

Gene >> PRICKLE2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64147486:64147486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754654816
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335Gln(p.R335Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64099403:64099403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2183G>A
AA Mutation	p.Arg728His(p.R728H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64147006:64147006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762969341
CDS Mutation	c.1484G>A
AA Mutation	p.Arg495Gln(p.R495Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64153271:64153271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698G>A
AA Mutation	p.Arg233His(p.R233H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64157281:64157281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773419206
CDS Mutation	c.481G>A
AA Mutation	p.Val161Ile(p.V161I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64147483:64147483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147289291
CDS Mutation	c.1007G>A
AA Mutation	p.Arg336His(p.R336H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64147132:64147132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767820294
CDS Mutation	c.1358C>T
AA Mutation	p.Ser453Leu(p.S453L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64099770:64099770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780001586
CDS Mutation	c.1816C>T
AA Mutation	p.Arg606Cys(p.R606C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64153203:64153203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766G>A
AA Mutation	p.Asp256Asn(p.D256N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64147385:64147385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568569832
CDS Mutation	c.1105G>A
AA Mutation	p.Val369Ile(p.V369I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64147502:64147502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778386656
CDS Mutation	c.988A>G
AA Mutation	p.Arg330Gly(p.R330G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64147657:64147657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>T
AA Mutation	p.Ala278Val(p.A278V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64099511:64099511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2075G>A
AA Mutation	p.Arg692His(p.R692H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64099473:64099473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766598630
CDS Mutation	c.2113C>T
AA Mutation	p.Arg705Cys(p.R705C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64147597:64147597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893T>C
AA Mutation	p.Leu298Pro(p.L298P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000295902
Start	64160023:64160023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313A>C
AA Mutation	p.Ser105Arg(p.S105R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295902
Start	64153234:64153234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295902
Start	64099213:64099213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2373A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295902
Start	64147395:64147395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1095G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295902
Start	64159991:64159991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148888682
CDS Mutation	c.345C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295902
Start	64099297:64099297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2289C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295902
Start	64099558:64099558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2028C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295902
Start	64153336:64153336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000295902
Start	64153332:64153332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637C>T
AA Mutation	p.Arg213Ter(p.R213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000295902
Start	64198782:64198782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript