Mutation

Primary Site >> Stomach Cancer

Gene >> PER3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7784914:7784914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37G>T
AA Mutation	p.Gly13Trp(p.G13W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7788132:7788132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478G>C
AA Mutation	p.Asp160His(p.D160H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7819335:7819335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549G>T
AA Mutation	p.Val517Leu(p.V517L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7827738:7827738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2785T>G
AA Mutation	p.Leu929Val(p.L929V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7827384:7827384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2431G>A
AA Mutation	p.Gly811Arg(p.G811R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7827571:7827571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2618C>T
AA Mutation	p.Ala873Val(p.A873V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7826542:7826542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1996T>C
AA Mutation	p.Ser666Pro(p.S666P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361923
Start	7827634:7827634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2681C>T
AA Mutation	p.Pro894Leu(p.P894L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361923
Start	7827146:7827146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369040184
CDS Mutation	c.2193G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361923
Start	7827272:7827272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2319C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361923
Start	7827764:7827764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2811C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361923
Start	7788194:7788194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535936436
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361923
Start	7801180:7801180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361923
Start	7826700:7826700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2154A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361923
Start	7827305:7827305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2352C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361923
Start	7798537:7798537(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.654delC
AA Mutation	p.Asp218GlufsTer17(p.D218Efs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000361923
Start	7803844:7803844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129C>T
AA Mutation	p.Arg377Ter(p.R377*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000361923
Start	7827804:7827804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2851C>T
AA Mutation	p.Gln951Ter(p.Q951*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript