Mutation

Primary Site >> Stomach Cancer

Gene >> BRD3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134048375:134048375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202191407
CDS Mutation	c.794C>T
AA Mutation	p.Pro265Leu(p.P265L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134053410:134053410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200460874
CDS Mutation	c.68C>A
AA Mutation	p.Pro23His(p.P23H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134045328:134045328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180G>T
AA Mutation	p.Asp394Tyr(p.D394Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134053389:134053389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89G>A
AA Mutation	p.Ser30Asn(p.S30N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134048223:134048223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946G>A
AA Mutation	p.Asp316Asn(p.D316N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134048318:134048318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851G>A
AA Mutation	p.Arg284His(p.R284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134041875:134041875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1292C>T
AA Mutation	p.Pro431Leu(p.P431L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134036293:134036293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759360626
CDS Mutation	c.1675G>A
AA Mutation	p.Ala559Thr(p.A559T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134036266:134036266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1702G>A
AA Mutation	p.Glu568Lys(p.E568K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134041857:134041857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1310C>T
AA Mutation	p.Ala437Val(p.A437V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134048178:134048178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991G>A
AA Mutation	p.Ala331Thr(p.A331T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134034737:134034737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202198193
CDS Mutation	c.2029G>A
AA Mutation	p.Gly677Arg(p.G677R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134052319:134052319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338A>G
AA Mutation	p.Tyr113Cys(p.Y113C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303407
Start	134041880:134041880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768208572
CDS Mutation	c.1287G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303407
Start	134036306:134036306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1662C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303407
Start	134048281:134048281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141698176
CDS Mutation	c.888C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303407
Start	134041928:134041928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201807714
CDS Mutation	c.1239C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303407
Start	134036309:134036309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752279707
CDS Mutation	c.1659C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303407
Start	134052421:134052421(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.236delA
AA Mutation	p.Asn79ThrfsTer12(p.N79Tfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303407
Start	134051653:134051653(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.408delA
AA Mutation	p.Val137TrpfsTer106(p.V137Wfs*106)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303407
Start	134036272:134036302(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1666_1696delCAGGCATCTGCCTCCTACGACTCAGAGGAAG
AA Mutation	p.Gln556ArgfsTer7(p.Q556Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303407
Start	134050444:134050444(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.644delC
AA Mutation	p.Pro215GlnfsTer28(p.P215Qfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript