Colon Cancer: Gene >> BRD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374825
Start	32976701:32976701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965G>A
AA Mutation	p.Arg322His(p.R322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374825
Start	32976700:32976700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964C>T
AA Mutation	p.Arg322Cys(p.R322C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374825
Start	32977871:32977871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444A>G
AA Mutation	p.Ser482Gly(p.S482G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374825
Start	32979985:32979985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1999C>T
AA Mutation	p.His667Tyr(p.H667Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374825
Start	32977570:32977570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329G>T
AA Mutation	p.Gln443His(p.Q443H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374825
Start	32977529:32977529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1288C>T
AA Mutation	p.Pro430Ser(p.P430S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374825
Start	32975394:32975394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752802138
CDS Mutation	c.344A>G
AA Mutation	p.Lys115Arg(p.K115R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374825
Start	32976841:32976841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105G>A
AA Mutation	p.Ala369Thr(p.A369T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374825
Start	32974618:32974618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374825
Start	32974555:32974555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374825
Start	32974545:32974548(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.113_116delTCTT
AA Mutation	p.Leu38ArgfsTer47(p.L38Rfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374825
Start	32978327:32978327(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1784delG
AA Mutation	p.Gly595ValfsTer6(p.G595Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000374825
Start	32977987:32977989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1562_1564delCAG
AA Mutation	p.Ala521del(p.A521del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BRD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374825
Start	32976306:32976306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200917553
CDS Mutation	c.667C>T
AA Mutation	p.His223Tyr(p.H223Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374825
Start	32980593:32980593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2281A>G
AA Mutation	p.Thr761Ala(p.T761A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript