Colon Cancer: Gene >> BMP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22201865:22201865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2170A>G
AA Mutation	p.Ser724Gly(p.S724G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22207366:22207366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200556837
CDS Mutation	c.2425G>A
AA Mutation	p.Asp809Asn(p.D809N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22176605:22176605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745868095
CDS Mutation	c.506G>A
AA Mutation	p.Arg169His(p.R169H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22173679:22173679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201377252
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Trp(p.R76W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22196703:22196703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1789A>G
AA Mutation	p.Lys597Glu(p.K597E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22176989:22176989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580G>A
AA Mutation	p.Gly194Arg(p.G194R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22176607:22176607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508A>G
AA Mutation	p.Thr170Ala(p.T170A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22195491:22195491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756176995
CDS Mutation	c.1669G>A
AA Mutation	p.Gly557Arg(p.G557R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22165499:22165499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>A
AA Mutation	p.Leu32Met(p.L32M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22194802:22194802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376781195
CDS Mutation	c.1522C>T
AA Mutation	p.Arg508Cys(p.R508C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22206970:22206970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202128760
CDS Mutation	c.2350C>T
AA Mutation	p.Arg784Trp(p.R784W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000306385
Start	22209445:22209445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2576A>T
AA Mutation	p.Glu859Val(p.E859V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22194769:22194769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146182213
CDS Mutation	c.1489G>A
AA Mutation	p.Asp497Asn(p.D497N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22173631:22173631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.178G>A
AA Mutation	p.Glu60Lys(p.E60K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000306385
Start	22179779:22179779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770440497
CDS Mutation	c.911G>A
AA Mutation	p.Arg304Gln(p.R304Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306385
Start	22197257:22197257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766899712
CDS Mutation	c.1944C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306385
Start	22209620:22209620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376975956
CDS Mutation	c.2751C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306385
Start	22176630:22176630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306385
Start	22177090:22177090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.681G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306385
Start	22209449:22209449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372744146
CDS Mutation	c.2580C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306385
Start	22196747:22196747(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778105011
CDS Mutation	c.1839delC
AA Mutation	p.Asn614ThrfsTer138(p.N614Tfs*138)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306385
Start	22207385:22207385(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2448delC
AA Mutation	p.Val817SerfsTer52(p.V817Sfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306385
Start	22176989:22176989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.584delG
AA Mutation	p.Gly195AlafsTer56(p.G195Afs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000306385
Start	22211681:22211681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773343328
CDS Mutation	c.2914C>T
AA Mutation	p.Arg972Ter(p.R972*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306385
Start	22196746:22196747(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1838_1839dupCC
AA Mutation	p.Asn614ProfsTer139(p.N614Pfs*139)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306385
Start	22196746:22196747(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs758822270
CDS Mutation	c.1839dupC
AA Mutation	p.Asn614GlnfsTer21(p.N614Qfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BMP1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306385
Start	22209644:22209644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541869451
CDS Mutation	c.2775C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306385
Start	22192141:22192141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76021885
CDS Mutation	c.1170G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306385
Start	22176160:22176161(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.285dupC
AA Mutation	p.Ser96GlnfsTer20(p.S96Qfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript