Mutation

Primary Site >> Stomach Cancer

Gene >> BCORL1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130025376:130025376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4075G>A
AA Mutation	p.Ala1359Thr(p.A1359T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130015534:130015534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2762C>A
AA Mutation	p.Pro921His(p.P921H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130014007:130014007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235C>T
AA Mutation	p.Pro412Leu(p.P412L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130015413:130015413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746950692
CDS Mutation	c.2641G>A
AA Mutation	p.Val881Met(p.V881M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130051935:130051935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4772T>C
AA Mutation	p.Met1591Thr(p.M1591T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130055973:130055973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4973G>T
AA Mutation	p.Arg1658Met(p.R1658M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130025050:130025050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3749T>C
AA Mutation	p.Phe1250Ser(p.F1250S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130051874:130051874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4711T>G
AA Mutation	p.Phe1571Val(p.F1571V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130021090:130021090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3547C>T
AA Mutation	p.Arg1183Trp(p.R1183W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130055879:130055879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367941726
CDS Mutation	c.4879G>A
AA Mutation	p.Asp1627Asn(p.D1627N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130015579:130015579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2807C>T
AA Mutation	p.Ser936Phe(p.S936F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130022965:130022965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3676C>G
AA Mutation	p.Arg1226Gly(p.R1226G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130025203:130025203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3902T>C
AA Mutation	p.Met1301Thr(p.M1301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130025116:130025116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3815A>G
AA Mutation	p.Gln1272Arg(p.Q1272R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130051977:130051977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4814T>G
AA Mutation	p.Leu1605Arg(p.L1605R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130028738:130028738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4182T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130056007:130056007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746115267
CDS Mutation	c.5007C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130013540:130013540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130013975:130013975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779766420
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130013354:130013354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130055932:130055932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4932G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130056036:130056036(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778658185
CDS Mutation	c.5042delC
AA Mutation	p.Pro1681GlnfsTer20(p.P1681Qfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130015204:130015204(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2432delC
AA Mutation	p.Ala811GlufsTer42(p.A811Efs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130014995:130014995(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2227delC
AA Mutation	p.Arg743AlafsTer40(p.R743Afs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130015446:130015446(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2678delG
AA Mutation	p.Gly893AlafsTer32(p.G893Afs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000218147
Start	130015164:130015164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2392C>T
AA Mutation	p.Gln798Ter(p.Q798*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130015767:130015768(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3001dupC
AA Mutation	p.Gln1001ProfsTer5(p.Q1001Pfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130013687:130013688(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.918_921dupAGTC
AA Mutation	p.Pro308SerfsTer113(p.P308Sfs*113)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript