Colon Cancer: Gene >> BMPR1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95129946:95129946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777745046
CDS Mutation	c.670C>T
AA Mutation	p.Arg224Cys(p.R224C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95114808:95114808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232G>A
AA Mutation	p.Asp78Asn(p.D78N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95131430:95131430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994G>A
AA Mutation	p.Asp332Asn(p.D332N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95154665:95154665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501A>G
AA Mutation	p.Lys501Glu(p.K501E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95114734:95114734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158G>T
AA Mutation	p.Cys53Phe(p.C53F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95131380:95131380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944T>C
AA Mutation	p.Leu315Ser(p.L315S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95104500:95104500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758706811
CDS Mutation	c.76C>T
AA Mutation	p.Arg26Cys(p.R26C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95148797:95148797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768328319
CDS Mutation	c.1126C>T
AA Mutation	p.Arg376Cys(p.R376C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95104495:95104495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.71C>T
AA Mutation	p.Thr24Ile(p.T24I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95115695:95115695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.257T>C
AA Mutation	p.Ile86Thr(p.I86T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264568
Start	95114821:95114821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245G>C
AA Mutation	p.Arg82Pro(p.R82P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95148890:95148890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1219C>A
AA Mutation	p.Leu407Ile(p.L407I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95115739:95115739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301G>A
AA Mutation	p.Glu101Lys(p.E101K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264568
Start	95131327:95131327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112111860
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264568
Start	95104495:95104495(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.76delC
AA Mutation	p.Arg26ValfsTer31(p.R26Vfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264568
Start	95114823:95114823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> BMPR1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95114769:95114769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>T
AA Mutation	p.Pro65Ser(p.P65S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264568
Start	95148822:95148822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1151A>G
AA Mutation	p.Asp384Gly(p.D384G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264568
Start	95129951:95129951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264568
Start	95114819:95114819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243T>C
Mutation Classification	Silent
Feature Type	Transcript