Colon Cancer: Gene >> BMP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57173204:57173204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142C>T
AA Mutation	p.Thr381Met(p.T381M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57228290:57228290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776230892
CDS Mutation	c.550C>T
AA Mutation	p.Arg184Cys(p.R184C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57228391:57228391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201575559
CDS Mutation	c.449G>A
AA Mutation	p.Arg150His(p.R150H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57228284:57228284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149261355
CDS Mutation	c.556G>A
AA Mutation	p.Asp186Asn(p.D186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57228323:57228323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>A
AA Mutation	p.Glu173Lys(p.E173K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57265732:57265732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.391G>A
AA Mutation	p.Asp131Asn(p.D131N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57173297:57173297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372973923
CDS Mutation	c.1049C>T
AA Mutation	p.Ala350Val(p.A350V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57183799:57183799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761254136
CDS Mutation	c.881C>T
AA Mutation	p.Thr294Met(p.T294M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57265989:57265989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Arg45His(p.R45H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57228316:57228316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755341380
CDS Mutation	c.524G>A
AA Mutation	p.Arg175Gln(p.R175Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57171086:57171086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766490422
CDS Mutation	c.1169C>T
AA Mutation	p.Thr390Met(p.T390M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57174966:57174966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772689429
CDS Mutation	c.1000G>A
AA Mutation	p.Glu334Lys(p.E334K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395863
Start	57173296:57173296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775245192
CDS Mutation	c.1050G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395863
Start	57183798:57183798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.882G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395863
Start	57183879:57183879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BMP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57228284:57228284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149261355
CDS Mutation	c.556G>A
AA Mutation	p.Asp186Asn(p.D186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395863
Start	57183785:57183785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Cys(p.R299C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript