Colon Cancer: Gene >> BCAR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93562375:93562375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2344T>A
AA Mutation	p.Phe782Ile(p.F782I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93571770:93571770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1874C>T
AA Mutation	p.Ala625Val(p.A625V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93674785:93674785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146G>A
AA Mutation	p.Gly49Asp(p.G49D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93567360:93567360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218A>G
AA Mutation	p.Met740Val(p.M740V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93567387:93567387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2191G>A
AA Mutation	p.Glu731Lys(p.E731K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93674630:93674630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370899092
CDS Mutation	c.301G>A
AA Mutation	p.Glu101Lys(p.E101K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93582317:93582317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1670T>G
AA Mutation	p.Leu557Arg(p.L557R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93571819:93571819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1825A>G
AA Mutation	p.Ile609Val(p.I609V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93589043:93589043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863G>T
AA Mutation	p.Arg288Met(p.R288M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260502
Start	93576082:93576082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1734G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260502
Start	93571742:93571742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776696865
CDS Mutation	c.1902G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260502
Start	93567380:93567380(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2198delA
AA Mutation	p.Asn733ThrfsTer9(p.N733Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BCAR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260502
Start	93674758:93674758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.173C>A
AA Mutation	p.Pro58His(p.P58H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260502
Start	93584112:93584112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000260502
Start	93582363:93582363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1624G>T
AA Mutation	p.Glu542Ter(p.E542*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript