Colon Cancer: Gene >> BMP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55755552:55755552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376923719
CDS Mutation	c.1346G>A
AA Mutation	p.Arg449His(p.R449H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55874489:55874489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144615410
CDS Mutation	c.377G>A
AA Mutation	p.Arg126His(p.R126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55760474:55760474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748959947
CDS Mutation	c.1087C>T
AA Mutation	p.Arg363Trp(p.R363W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55755553:55755553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752442881
CDS Mutation	c.1345C>T
AA Mutation	p.Arg449Cys(p.R449C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55755666:55755666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232C>A
AA Mutation	p.Pro411His(p.P411H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55774213:55774213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.863T>G
AA Mutation	p.Leu288Arg(p.L288R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370830
Start	55760532:55760532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029T>G
AA Mutation	p.Asp343Glu(p.D343E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55819796:55819796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.542G>T
AA Mutation	p.Arg181Leu(p.R181L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370830
Start	55874647:55874647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370830
Start	55774155:55774155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575324695
CDS Mutation	c.921G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370830
Start	55774134:55774134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747912353
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000370830
Start	55774115:55774115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550837639
CDS Mutation	c.961C>T
AA Mutation	p.Arg321Ter(p.R321*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BMP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55874590:55874590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276A>C
AA Mutation	p.Glu92Asp(p.E92D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55774099:55774099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371743666
CDS Mutation	c.977G>A
AA Mutation	p.Arg326His(p.R326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370830
Start	55759060:55759060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1160C>A
AA Mutation	p.Ser387Tyr(p.S387Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript