Colon Cancer: Gene >> BRS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370648
Start	136490477:136490477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376207740
CDS Mutation	c.779G>A
AA Mutation	p.Arg260His(p.R260H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370648
Start	136490209:136490209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752869358
CDS Mutation	c.511G>A
AA Mutation	p.Val171Ile(p.V171I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370648
Start	136492284:136492284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750000912
CDS Mutation	c.1109C>T
AA Mutation	p.Thr370Met(p.T370M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370648
Start	136490351:136490351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653C>A
AA Mutation	p.Ser218Tyr(p.S218Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370648
Start	136492340:136492340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1165G>T
AA Mutation	p.Gly389Trp(p.G389W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370648
Start	136488437:136488437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323A>G
AA Mutation	p.Tyr108Cys(p.Y108C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370648
Start	136490217:136490217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202114962
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370648
Start	136490412:136490412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000370648
Start	136488247:136488247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133G>T
AA Mutation	p.Glu45Ter(p.E45*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BRS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370648
Start	136488464:136488464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350G>A
AA Mutation	p.Arg117Lys(p.R117K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370648
Start	136492182:136492182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007G>T
AA Mutation	p.Ser336Ile(p.S336I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370648
Start	136488327:136488327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213C>A
Mutation Classification	Silent
Feature Type	Transcript