Colon Cancer: Gene >> BMP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81046026:81046026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605T>A
AA Mutation	p.Ile202Asn(p.I202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81046451:81046451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030C>T
AA Mutation	p.Arg344Trp(p.R344W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81046175:81046175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754C>T
AA Mutation	p.Pro252Ser(p.P252S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81046008:81046008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587C>T
AA Mutation	p.Ser196Phe(p.S196F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81031490:81031490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206C>T
AA Mutation	p.Thr69Met(p.T69M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81046272:81046272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751449569
CDS Mutation	c.851A>T
AA Mutation	p.Glu284Val(p.E284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282701
Start	81031332:81031332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282701
Start	81046490:81046490(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1073delA
AA Mutation	p.Lys358ArgfsTer20(p.K358Rfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000282701
Start	81031429:81031429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145G>T
AA Mutation	p.Glu49Ter(p.E49*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000282701
Start	81031435:81031435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>T
AA Mutation	p.Gln51Ter(p.Q51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BMP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81046464:81046464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145297209
CDS Mutation	c.1043C>T
AA Mutation	p.Thr348Met(p.T348M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81046451:81046451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030C>T
AA Mutation	p.Arg344Trp(p.R344W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81046160:81046160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.739G>T
AA Mutation	p.Ala247Ser(p.A247S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282701
Start	81031444:81031444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>T
AA Mutation	p.Asp54Tyr(p.D54Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282701
Start	81031359:81031359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150246562
CDS Mutation	c.75G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282701
Start	81046036:81046036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.615C>A
Mutation Classification	Silent
Feature Type	Transcript