Mutation

Primary Site >> Stomach Cancer

Gene >> PPP1R13L

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45396620:45396620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637G>A
AA Mutation	p.Ala213Thr(p.A213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45398039:45398039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768668757
CDS Mutation	c.164C>T
AA Mutation	p.Ala55Val(p.A55V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45398027:45398027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176C>T
AA Mutation	p.Pro59Leu(p.P59L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45396719:45396719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538C>T
AA Mutation	p.Arg180Cys(p.R180C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45396421:45396421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752605602
CDS Mutation	c.728G>A
AA Mutation	p.Arg243His(p.R243H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45382685:45382685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2290T>C
AA Mutation	p.Tyr764His(p.Y764H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45382541:45382541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763548265
CDS Mutation	c.2434C>T
AA Mutation	p.Arg812Trp(p.R812W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45382617:45382617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2358C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45391991:45391991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45396375:45396375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45396408:45396408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372976271
CDS Mutation	c.741G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45385608:45385608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2202C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45391916:45391916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148594569
CDS Mutation	c.1779G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45396624:45396624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45398292:45398292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45392303:45392303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767546785
CDS Mutation	c.1392G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360957
Start	45396915:45396915(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.342delC
AA Mutation	p.Lys115ArgfsTer109(p.K115Rfs*109)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360957
Start	45396178:45396178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.893delG
AA Mutation	p.Gly298AlafsTer77(p.G298Afs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360957
Start	45392012:45392012(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1683delG
AA Mutation	p.Pro562ArgfsTer75(p.P562Rfs*75)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360957
Start	45397000:45397001(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.256dupC
AA Mutation	p.Arg86ProfsTer169(p.R86Pfs*169)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript