Colon Cancer: Gene >> BRD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15239065:15239065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3776G>A
AA Mutation	p.Arg1259His(p.R1259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15244316:15244316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2496G>T
AA Mutation	p.Gln832His(p.Q832H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15265578:15265578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201864530
CDS Mutation	c.625C>G
AA Mutation	p.Gln209Glu(p.Q209E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15256097:15256097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150583855
CDS Mutation	c.1718C>T
AA Mutation	p.Thr573Met(p.T573M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15239402:15239402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368540009
CDS Mutation	c.3566C>T
AA Mutation	p.Ala1189Val(p.A1189V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15238778:15238778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3985C>T
AA Mutation	p.Arg1329Trp(p.R1329W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15255450:15255450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1894C>T
AA Mutation	p.Arg632Cys(p.R632C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15239155:15239155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3686G>A
AA Mutation	p.Arg1229His(p.R1229H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15239742:15239742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3362G>A
AA Mutation	p.Arg1121His(p.R1121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15244366:15244366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760576705
CDS Mutation	c.2446G>A
AA Mutation	p.Val816Ile(p.V816I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15256239:15256239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1576G>A
AA Mutation	p.Ala526Thr(p.A526T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15273044:15273044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56A>G
AA Mutation	p.Asp19Gly(p.D19G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15239212:15239212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3629C>T
AA Mutation	p.Pro1210Leu(p.P1210L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15257053:15257053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462A>G
AA Mutation	p.Ser488Gly(p.S488G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15243034:15243034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749938247
CDS Mutation	c.3035C>T
AA Mutation	p.Pro1012Leu(p.P1012L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15272834:15272834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266C>T
AA Mutation	p.Ala89Val(p.A89V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15256086:15256086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1729A>G
AA Mutation	p.Asn577Asp(p.N577D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15264688:15264688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Pro310Ser(p.P310S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15265388:15265388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815C>T
AA Mutation	p.Pro272Leu(p.P272L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15263500:15263500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261G>C
AA Mutation	p.Asp421His(p.D421H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263377
Start	15256240:15256240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1575T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263377
Start	15256231:15256231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1584C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263377
Start	15265627:15265627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763875252
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263377
Start	15257165:15257165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201699426
CDS Mutation	c.1350C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000263377
Start	15263494:15263494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267C>T
AA Mutation	p.Arg423Ter(p.R423*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000263377
Start	15255387:15255387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1957G>T
AA Mutation	p.Glu653Ter(p.E653*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BRD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15255425:15255425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1919G>A
AA Mutation	p.Arg640Gln(p.R640Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263377
Start	15239995:15239995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3197T>C
AA Mutation	p.Leu1066Pro(p.L1066P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263377
Start	15273085:15273085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147477529
CDS Mutation	c.15C>T
Mutation Classification	Silent
Feature Type	Transcript