Mutation

Primary Site >> Stomach Cancer

Gene >> VPS13C

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61981385:61981385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2123A>C
AA Mutation	p.His708Pro(p.H708P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61873352:61873352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10472C>T
AA Mutation	p.Ala3491Val(p.A3491V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261517
Start	61945882:61945882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4981G>A
AA Mutation	p.Ala1661Thr(p.A1661T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61927222:61927222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6385A>G
AA Mutation	p.Thr2129Ala(p.T2129A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61925511:61925511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146858303
CDS Mutation	c.6554C>T
AA Mutation	p.Thr2185Met(p.T2185M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61945722:61945722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5141C>T
AA Mutation	p.Ser1714Phe(p.S1714F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	62012124:62012124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200657349
CDS Mutation	c.866C>A
AA Mutation	p.Pro289His(p.P289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61854521:61854521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11198G>A
AA Mutation	p.Arg3733Lys(p.R3733K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61863517:61863517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10875A>C
AA Mutation	p.Lys3625Asn(p.K3625N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61910286:61910286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8735A>C
AA Mutation	p.Glu2912Ala(p.E2912A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61922491:61922491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560778934
CDS Mutation	c.6881G>A
AA Mutation	p.Arg2294Gln(p.R2294Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	62035011:62035011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202047135
CDS Mutation	c.229G>A
AA Mutation	p.Glu77Lys(p.E77K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61890346:61890346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9160T>A
AA Mutation	p.Phe3054Ile(p.F3054I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61959575:61959575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3929T>C
AA Mutation	p.Ile1310Thr(p.I1310T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61961655:61961655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3842A>G
AA Mutation	p.Glu1281Gly(p.E1281G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61963946:61963946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3220G>A
AA Mutation	p.Val1074Ile(p.V1074I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61890310:61890310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775795504
CDS Mutation	c.9196G>A
AA Mutation	p.Asp3066Asn(p.D3066N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61873362:61873362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10462G>T
AA Mutation	p.Gly3488Cys(p.G3488C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61910217:61910217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8804A>T
AA Mutation	p.Asn2935Ile(p.N2935I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261517
Start	61880845:61880845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377118536
CDS Mutation	c.9886C>T
AA Mutation	p.Arg3296Trp(p.R3296W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61982498:61982498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1990T>G
AA Mutation	p.Leu664Val(p.L664V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61922455:61922455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6917C>T
AA Mutation	p.Ser2306Leu(p.S2306L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61972759:61972759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2623G>C
AA Mutation	p.Asp875His(p.D875H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000261517
Start	61945724:61945724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5139G>A
AA Mutation	p.Met1713Ile(p.M1713I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261517
Start	62010474:62010474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760175192
CDS Mutation	c.1009C>G
AA Mutation	p.Gln337Glu(p.Q337E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261517
Start	61917379:61917379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752109410
CDS Mutation	c.8017C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261517
Start	61863454:61863454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10938T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261517
Start	61915954:61915954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8124T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261517
Start	61951966:61951966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4314G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261517
Start	61915913:61915913(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.8165delA
AA Mutation	p.Asn2722ThrfsTer27(p.N2722Tfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261517
Start	61964716:61964716(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3197delA
AA Mutation	p.Asn1066IlefsTer25(p.N1066Ifs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000261517
Start	61920124:61920124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7420C>T
AA Mutation	p.Gln2474Ter(p.Q2474*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000261517
Start	61911965:61911965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751495707
CDS Mutation	c.8590C>T
AA Mutation	p.Arg2864Ter(p.R2864*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000261517
Start	61856408:61856408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138846118
CDS Mutation	c.10954C>T
AA Mutation	p.Arg3652Ter(p.R3652*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000261517
Start	62033519:62033519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307G>T
AA Mutation	p.Glu103Ter(p.E103*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000261517
Start	61880935:61880935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9796C>T
AA Mutation	p.Gln3266Ter(p.Q3266*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000261517
Start	61873248:61873248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779001393
CDS Mutation	c.10576C>T
AA Mutation	p.Arg3526Ter(p.R3526*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261517
Start	61890314:61890315(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.9191dupT
AA Mutation	p.Thr3065HisfsTer3(p.T3065Hfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261517
Start	61890260:61890261(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.9245_9246insCTTTCTTCAAATC
AA Mutation	p.Gln3082HisfsTer7(p.Q3082Hfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261517
Start	61951850:61951851(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4429dupA
AA Mutation	p.Ile1477AsnfsTer2(p.I1477Nfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	41
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000261517
Start	61854869:61854869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11160+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	42
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000261517
Start	61950943:61950943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4536+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript