Colon Cancer: Gene >> BMP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950195:53950195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064C>T
AA Mutation	p.Ala355Val(p.A355V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53952018:53952018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Cys(p.R69C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950105:53950105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154A>G
AA Mutation	p.Tyr385Cys(p.Y385C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950492:53950492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746984770
CDS Mutation	c.767G>A
AA Mutation	p.Arg256Gln(p.R256Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950844:53950844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753312749
CDS Mutation	c.415C>T
AA Mutation	p.Arg139Cys(p.R139C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950164:53950164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095T>G
AA Mutation	p.Asn365Lys(p.N365K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950333:53950333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778657318
CDS Mutation	c.926G>A
AA Mutation	p.Arg309Gln(p.R309Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245451
Start	53950422:53950422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000245451
Start	53951882:53951893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.330_341delGGCCAGCCGGGC
AA Mutation	p.Ala111_Ala114del(p.A111_A114del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BMP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950081:53950081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178T>C
AA Mutation	p.Val393Ala(p.V393A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950628:53950628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748940819
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Trp(p.R211W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript