Colon Cancer: Gene >> BRD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134052320:134052320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337T>A
AA Mutation	p.Tyr113Asn(p.Y113N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134036212:134036212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1756C>T
AA Mutation	p.Arg586Trp(p.R586W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134048184:134048184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985G>A
AA Mutation	p.Ala329Thr(p.A329T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
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

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134053440:134053440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370821220
CDS Mutation	c.38C>T
AA Mutation	p.Pro13Leu(p.P13L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134053354:134053354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124A>G
AA Mutation	p.Met42Val(p.M42V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134045391:134045391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775918544
CDS Mutation	c.1117G>A
AA Mutation	p.Ala373Thr(p.A373T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000303407
Start	134051603:134051603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458A>G
AA Mutation	p.Lys153Arg(p.K153R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
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

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303407
Start	134050545:134050545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303407
Start	134041847:134041847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1320C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
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

Mutation ID	13
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

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303407
Start	134053407:134053407(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763134487
CDS Mutation	c.71delC
AA Mutation	p.Pro24ArgfsTer24(p.P24Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000303407
Start	134045406:134045406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102C>T
AA Mutation	p.Arg368Ter(p.R368*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BRD3

Mutation ID	1
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

Mutation ID	2
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000303407
Start	134040177:134040191(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771963978
CDS Mutation	c.1486_1500delGAGAAGGAGAAGAAG
AA Mutation	p.Glu496_Lys500del(p.E496_K500del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript