Mutation

Primary Site >> Stomach Cancer

Gene >> CCKBR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270231:6270231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547G>A
AA Mutation	p.Gly183Arg(p.G183R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270307:6270307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775117809
CDS Mutation	c.623G>A
AA Mutation	p.Arg208His(p.R208H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271109:6271109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.910C>A
AA Mutation	p.Leu304Met(p.L304M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270138:6270138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777692103
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Trp(p.R152W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270306:6270306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Cys(p.R208C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6269768:6269768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145658504
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271140:6271140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201626406
CDS Mutation	c.941C>T
AA Mutation	p.Pro314Leu(p.P314L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271128:6271128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929C>T
AA Mutation	p.Thr310Met(p.T310M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270129:6270129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445G>A
AA Mutation	p.Ala149Thr(p.A149T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270752:6270752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760G>A
AA Mutation	p.Asp254Asn(p.D254N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271470:6271470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1271A>G
AA Mutation	p.Asp424Gly(p.D424G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271118:6271118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919A>G
AA Mutation	p.Thr307Ala(p.T307A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270319:6270319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635C>T
AA Mutation	p.Ala212Val(p.A212V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6271495:6271495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6270254:6270254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6271054:6271054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149197660
CDS Mutation	c.855G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6269700:6269700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6269835:6269835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6270122:6270122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6271069:6271069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334619
Start	6271356:6271357(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1162dupC
AA Mutation	p.Leu388ProfsTer36(p.L388Pfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334619
Start	6271168:6271169(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.971dupA
AA Mutation	p.Leu325AlafsTer4(p.L325Afs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript