Mutation

Primary Site >> Stomach Cancer

Gene >> RPTOR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80625746:80625746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>A
AA Mutation	p.Pro73His(p.P73H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80908853:80908853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2444T>C
AA Mutation	p.Leu815Pro(p.L815P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80891736:80891736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2000T>C
AA Mutation	p.Leu667Pro(p.L667P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80883913:80883913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775264665
CDS Mutation	c.1783G>A
AA Mutation	p.Gly595Ser(p.G595S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80823135:80823135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048T>G
AA Mutation	p.Phe350Val(p.F350V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80730681:80730681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745951041
CDS Mutation	c.629C>T
AA Mutation	p.Ala210Val(p.A210V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80822281:80822281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748079762
CDS Mutation	c.971C>T
AA Mutation	p.Ala324Val(p.A324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80880464:80880464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1559C>T
AA Mutation	p.Ser520Leu(p.S520L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80891756:80891756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768927275
CDS Mutation	c.2020T>C
AA Mutation	p.Tyr674His(p.Y674H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80908849:80908849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2440G>T
AA Mutation	p.Val814Phe(p.V814F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80754178:80754178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823C>A
AA Mutation	p.Leu275Met(p.L275M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80923501:80923501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2636C>T
AA Mutation	p.Pro879Leu(p.P879L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80885066:80885066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1901C>T
AA Mutation	p.Thr634Met(p.T634M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80730680:80730680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560409938
CDS Mutation	c.628G>A
AA Mutation	p.Ala210Thr(p.A210T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80855506:80855506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1357C>T
AA Mutation	p.Leu453Phe(p.L453F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000306801
Start	80883871:80883871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1741C>T
AA Mutation	p.Leu581Phe(p.L581F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80625717:80625717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80754132:80754132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138893220
CDS Mutation	c.777G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80960173:80960173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532712262
CDS Mutation	c.3573C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80730568:80730568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747545472
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80964309:80964309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769703866
CDS Mutation	c.3987G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80960161:80960161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565225948
CDS Mutation	c.3561C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80962563:80962563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777256656
CDS Mutation	c.3795G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80925441:80925441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772995479
CDS Mutation	c.2880C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306801
Start	80893714:80893714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115028103
CDS Mutation	c.2250C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306801
Start	80891767:80891767(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2033delT
AA Mutation	p.Phe678SerfsTer9(p.F678Sfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000306801
Start	80891795:80891795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2059G>T
AA Mutation	p.Glu687Ter(p.E687*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000306801
Start	80892871:80892871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2242+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript