Colon Cancer: Gene >> BRD1

Mutation ID	1
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

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49775597:49775597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2987G>T
AA Mutation	p.Arg996Ile(p.R996I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49797975:49797975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1928C>T
AA Mutation	p.Ala643Val(p.A643V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49774373:49774373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3037G>A
AA Mutation	p.Glu1013Lys(p.E1013K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49777733:49777733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2545C>T
AA Mutation	p.Arg849Cys(p.R849C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823218:49823218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100T>C
AA Mutation	p.Val367Ala(p.V367A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49777108:49777108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780837839
CDS Mutation	c.2654C>T
AA Mutation	p.Thr885Met(p.T885M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49777153:49777153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764535212
CDS Mutation	c.2609C>T
AA Mutation	p.Ala870Val(p.A870V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823702:49823702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616G>A
AA Mutation	p.Glu206Lys(p.E206K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823651:49823651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667G>A
AA Mutation	p.Gly223Arg(p.G223R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49824241:49824241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77C>A
AA Mutation	p.Pro26His(p.P26H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49799053:49799053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781108454
CDS Mutation	c.1591G>A
AA Mutation	p.Asp531Asn(p.D531N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49777139:49777139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2623C>T
AA Mutation	p.Arg875Trp(p.R875W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49777096:49777096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757367533
CDS Mutation	c.2666G>A
AA Mutation	p.Arg889His(p.R889H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49797829:49797829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2074C>T
AA Mutation	p.Arg692Trp(p.R692W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49775739:49775739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750190219
CDS Mutation	c.2845G>A
AA Mutation	p.Asp949Asn(p.D949N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49787450:49787450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2404C>T
AA Mutation	p.Arg802Trp(p.R802W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49799017:49799017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774744137
CDS Mutation	c.1627C>T
AA Mutation	p.Arg543Cys(p.R543C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49804244:49804244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1484G>T
AA Mutation	p.Arg495Leu(p.R495L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216267
Start	49823727:49823727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376636833
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216267
Start	49823862:49823862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142139061
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216267
Start	49823023:49823023(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1295delA
AA Mutation	p.Lys432ArgfsTer26(p.K432Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000216267
Start	49824293:49824293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25C>T
AA Mutation	p.Arg9Ter(p.R9*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BRD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823510:49823510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>A
AA Mutation	p.Asp270Asn(p.D270N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49775596:49775596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2988A>T
AA Mutation	p.Arg996Ser(p.R996S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216267
Start	49823375:49823375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943G>A
AA Mutation	p.Val315Met(p.V315M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216267
Start	49774358:49774358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3052T>C
Mutation Classification	Silent
Feature Type	Transcript