Mutation

Primary Site >> Stomach Cancer

Gene >> BRD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823543:49823543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775C>T
AA Mutation	p.Arg259Cys(p.R259C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823986:49823986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779060123
CDS Mutation	c.332C>T
AA Mutation	p.Pro111Leu(p.P111L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49776069:49776069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2819A>G
AA Mutation	p.Tyr940Cys(p.Y940C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49804331:49804331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397T>C
AA Mutation	p.Ile466Thr(p.I466T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823968:49823968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350T>G
AA Mutation	p.Leu117Arg(p.L117R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823542:49823542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776G>A
AA Mutation	p.Arg259His(p.R259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823597:49823597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753570026
CDS Mutation	c.721G>A
AA Mutation	p.Val241Met(p.V241M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823819:49823819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776625246
CDS Mutation	c.499G>A
AA Mutation	p.Glu167Lys(p.E167K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49776055:49776055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2833G>A
AA Mutation	p.Ala945Thr(p.A945T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49774276:49774276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3134G>A
AA Mutation	p.Arg1045His(p.R1045H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823879:49823879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439G>A
AA Mutation	p.Ala147Thr(p.A147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49797964:49797964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751309590
CDS Mutation	c.1939G>A
AA Mutation	p.Val647Met(p.V647M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49794132:49794132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2261A>G
AA Mutation	p.Lys754Arg(p.K754R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823818:49823818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500A>T
AA Mutation	p.Glu167Val(p.E167V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823570:49823570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748T>C
AA Mutation	p.Tyr250His(p.Y250H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49804263:49804263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465G>A
AA Mutation	p.Gly489Arg(p.G489R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823053:49823053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1265C>A
AA Mutation	p.Ser422Tyr(p.S422Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49799043:49799043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367857228
CDS Mutation	c.1601G>A
AA Mutation	p.Arg534His(p.R534H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49794076:49794076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2317G>A
AA Mutation	p.Glu773Lys(p.E773K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216267
Start	49824219:49824219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149523607
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216267
Start	49774317:49774317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144418668
CDS Mutation	c.3093C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216267
Start	49822983:49822983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758434485
CDS Mutation	c.1335G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216267
Start	49823562:49823562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538087121
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216267
Start	49823919:49823919(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.399delC
AA Mutation	p.Arg134GlyfsTer56(p.R134Gfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216267
Start	49775657:49775658(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2926dupG
AA Mutation	p.Glu976GlyfsTer8(p.E976Gfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000216267
Start	49798688:49798688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1657-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	27
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000216267
Start	49823196:49823201(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1117_1122delGGTGGC
AA Mutation	p.Gly373_Gly374del(p.G373_G374del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript