Colon Cancer: Gene >> BRD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000467963
Start	878386:878386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240G>A
AA Mutation	p.Gly414Arg(p.G414R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000467963
Start	891709:891709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.198G>T
AA Mutation	p.Lys66Asn(p.K66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000467963
Start	891286:891286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269A>G
AA Mutation	p.Glu90Gly(p.E90G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000467963
Start	881122:881122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144680205
CDS Mutation	c.1027G>A
AA Mutation	p.Glu343Lys(p.E343K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000467963
Start	884032:884032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748289899
CDS Mutation	c.872C>T
AA Mutation	p.Thr291Met(p.T291M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000467963
Start	891804:891804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103G>A
AA Mutation	p.Gly35Arg(p.G35R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000467963
Start	884021:884021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883G>A
AA Mutation	p.Ala295Thr(p.A295T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000467963
Start	864557:864557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758871899
CDS Mutation	c.1705C>T
AA Mutation	p.Arg569Cys(p.R569C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467963
Start	891661:891661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467963
Start	864531:864531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141705577
CDS Mutation	c.1731C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000467963
Start	891176:891176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379C>T
AA Mutation	p.Arg127Ter(p.R127*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BRD9

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000467963
Start	889022:889022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605A>G
AA Mutation	p.Lys202Arg(p.K202R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000467963
Start	889129:889129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript