Mutation

Primary Site >> Stomach Cancer

Gene >> FCRL3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157695374:157695374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1366G>T
AA Mutation	p.Gly456Cys(p.G456C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157695352:157695352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1388A>C
AA Mutation	p.His463Pro(p.H463P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157695565:157695565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1175C>G
AA Mutation	p.Ala392Gly(p.A392G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157697701:157697701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517G>C
AA Mutation	p.Asp173His(p.D173H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157697775:157697775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443A>G
AA Mutation	p.Lys148Arg(p.K148R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157697342:157697342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642G>C
AA Mutation	p.Gln214His(p.Q214H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157698494:157698494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188A>C
AA Mutation	p.Lys63Thr(p.K63T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157696151:157696151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759624449
CDS Mutation	c.1021G>A
AA Mutation	p.Ala341Thr(p.A341T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157697225:157697225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759A>C
AA Mutation	p.Glu253Asp(p.E253D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157696295:157696295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146153982
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Trp(p.R293W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157698515:157698515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167C>T
AA Mutation	p.Thr56Ile(p.T56I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157696118:157696118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054G>A
AA Mutation	p.Asp352Asn(p.D352N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157698411:157698411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>A
AA Mutation	p.Asp91Asn(p.D91N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157696112:157696112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060G>T
AA Mutation	p.Gly354Trp(p.G354W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157697838:157697838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380A>C
AA Mutation	p.Asn127Thr(p.N127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157698548:157698548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Ser45Asn(p.S45N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000368184
Start	157697666:157697666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552A>C
AA Mutation	p.Gln184His(p.Q184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368184
Start	157696277:157696277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368184
Start	157690409:157690409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141302640
CDS Mutation	c.1536C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368184
Start	157697696:157697696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368184
Start	157697170:157697170(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.814delA
AA Mutation	p.Arg272GlyfsTer3(p.R272Gfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368184
Start	157696219:157696220(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.952_953delGT
AA Mutation	p.Val318HisfsTer15(p.V318Hfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368184
Start	157690291:157690291(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1654delG
AA Mutation	p.Ala552ProfsTer7(p.A552Pfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368184
Start	157697169:157697170(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.814dupA
AA Mutation	p.Arg272LysfsTer16(p.R272Kfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000368184
Start	157698631:157698631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript