Mutation

Primary Site >> Stomach Cancer

Gene >> RICTOR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38945497:38945497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4627C>T
AA Mutation	p.His1543Tyr(p.H1543Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38958749:38958749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2261T>C
AA Mutation	p.Leu754Ser(p.L754S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38945652:38945652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4472A>C
AA Mutation	p.Glu1491Ala(p.E1491A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38942882:38942882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77464125
CDS Mutation	c.5003C>T
AA Mutation	p.Pro1668Leu(p.P1668L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38947437:38947437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4141A>G
AA Mutation	p.Met1381Val(p.M1381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38952354:38952354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2969G>C
AA Mutation	p.Trp990Ser(p.W990S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38959203:38959203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2170G>A
AA Mutation	p.Ala724Thr(p.A724T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	39002569:39002569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>T
AA Mutation	p.Val120Leu(p.V120L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38950201:38950201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3647G>A
AA Mutation	p.Arg1216His(p.R1216H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38967997:38967997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006C>T
AA Mutation	p.Arg336Cys(p.R336C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38947331:38947331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371275210
CDS Mutation	c.4247C>T
AA Mutation	p.Ala1416Val(p.A1416V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38967352:38967352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1136A>G
AA Mutation	p.His379Arg(p.H379R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38947317:38947317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4261T>C
AA Mutation	p.Ser1421Pro(p.S1421P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	38950519:38950519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766067681
CDS Mutation	c.3329G>A
AA Mutation	p.Arg1110His(p.R1110H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000357387
Start	39002604:39002604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323G>A
AA Mutation	p.Arg108Gln(p.R108Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357387
Start	38959826:38959826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2004C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357387
Start	39002597:39002597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357387
Start	38960443:38960443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760985733
CDS Mutation	c.1806G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357387
Start	38945691:38945691(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4433delA
AA Mutation	p.Asn1478IlefsTer10(p.N1478Ifs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357387
Start	38959848:38959848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1982delT
AA Mutation	p.Leu661TyrfsTer31(p.L661Yfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357387
Start	38945613:38945613(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4511delT
AA Mutation	p.Leu1504Ter(p.L1504*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357387
Start	38975570:38975570(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.856delA
AA Mutation	p.Met286TrpfsTer4(p.M286Wfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000357387
Start	38963040:38963040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200068996
CDS Mutation	c.1402C>T
AA Mutation	p.Arg468Ter(p.R468*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000357387
Start	38975588:38975588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838C>T
AA Mutation	p.Arg280Ter(p.R280*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000357387
Start	38981887:38981887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Ter(p.R245*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357387
Start	38959925:38959926(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1904dupA
AA Mutation	p.Asn635LysfsTer15(p.N635Kfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000357387
Start	38964894:38964894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1300-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript