Mutation

Primary Site >> Stomach Cancer

Gene >> NCOR1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16032427:16032427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7192C>T
AA Mutation	p.Pro2398Ser(p.P2398S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16108797:16108797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2171A>T
AA Mutation	p.Glu724Val(p.E724V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16101494:16101494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76080188
CDS Mutation	c.2446G>A
AA Mutation	p.Ala816Thr(p.A816T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16086428:16086428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3031C>T
AA Mutation	p.Pro1011Ser(p.P1011S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16137374:16137374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1446G>T
AA Mutation	p.Lys482Asn(p.K482N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16119435:16119435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1903G>A
AA Mutation	p.Val635Ile(p.V635I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16091971:16091971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2908T>C
AA Mutation	p.Ser970Pro(p.S970P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16171927:16171927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311T>C
AA Mutation	p.Leu104Pro(p.L104P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16138184:16138184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381C>A
AA Mutation	p.Leu461Ile(p.L461I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16121099:16121099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749634427
CDS Mutation	c.1805C>T
AA Mutation	p.Ala602Val(p.A602V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16138181:16138181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1384A>G
AA Mutation	p.Ile462Val(p.I462V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16061889:16061889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5393T>A
AA Mutation	p.Leu1798Gln(p.L1798Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16067968:16067968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4667C>T
AA Mutation	p.Ala1556Val(p.A1556V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16070426:16070426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4252C>T
AA Mutation	p.Pro1418Ser(p.P1418S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16121136:16121136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1768A>G
AA Mutation	p.Thr590Ala(p.T590A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16098441:16098441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781456795
CDS Mutation	c.2746G>A
AA Mutation	p.Val916Ile(p.V916I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16061799:16061799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5483C>T
AA Mutation	p.Ala1828Val(p.A1828V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16139122:16139122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238G>A
AA Mutation	p.Arg413Lys(p.R413K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16121153:16121153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1751G>A
AA Mutation	p.Arg584Gln(p.R584Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16064130:16064130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759534850
CDS Mutation	c.5159G>A
AA Mutation	p.Arg1720Gln(p.R1720Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16065623:16065623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762318164
CDS Mutation	c.4813G>A
AA Mutation	p.Ala1605Thr(p.A1605T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000268712
Start	16071441:16071441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4120A>G
AA Mutation	p.Thr1374Ala(p.T1374A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16101495:16101495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139942816
CDS Mutation	c.2445C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16101645:16101645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2295C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16039443:16039443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6945A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16068074:16068074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4561C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16165114:16165114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16068042:16068042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771741474
CDS Mutation	c.4593G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16138164:16138164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16057964:16057964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6111G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16065504:16065504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4932C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16121131:16121131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761000533
CDS Mutation	c.1773C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16032311:16032311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7308G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16071438:16071438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4123C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16121098:16121098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778137445
CDS Mutation	c.1806G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16068012:16068012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369446328
CDS Mutation	c.4623C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16070193:16070193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4485C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16086360:16086360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747290065
CDS Mutation	c.3099G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268712
Start	16058532:16058532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5949G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268712
Start	16072200:16072200(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3840delG
AA Mutation	p.Ser1281ValfsTer16(p.S1281Vfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000268712
Start	16137373:16137373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1447A>T
AA Mutation	p.Lys483Ter(p.K483*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	stop_gained
Transcription ID	ENST00000268712
Start	16080471:16080471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3337C>T
AA Mutation	p.Arg1113Ter(p.R1113*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	stop_gained
Transcription ID	ENST00000268712
Start	16121190:16121190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1714C>T
AA Mutation	p.Arg572Ter(p.R572*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000268712
Start	16119423:16119424(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1914dupA
AA Mutation	p.Gly639ArgfsTer8(p.G639Rfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268712
Start	16067939:16067940(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4695dupC
AA Mutation	p.Thr1566HisfsTer51(p.T1566Hfs*51)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	46
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000268712
Start	16146374:16146374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	47
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000268712
Start	16101269:16101274(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2666_2671delTGGATG
AA Mutation	p.Val889_Asp890del(p.V889_D890del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript