Colon Cancer: Gene >> SMAD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379826
Start	36853487:36853487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1192G>C
AA Mutation	p.Val398Leu(p.V398L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379826
Start	36879401:36879401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289C>A
AA Mutation	p.Arg97Ser(p.R97S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379826
Start	36879401:36879401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Cys(p.R97C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379826
Start	36879407:36879407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Val95Met(p.V95M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379826
Start	36853508:36853508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148698551
CDS Mutation	c.1171G>A
AA Mutation	p.Ala391Thr(p.A391T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379826
Start	36879439:36879439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759141619
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379826
Start	36865716:36865716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368154262
CDS Mutation	c.824C>T
AA Mutation	p.Ser275Leu(p.S275L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379826
Start	36867374:36867374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.680C>A
AA Mutation	p.Pro227Gln(p.P227Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379826
Start	36867286:36867286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372254094
CDS Mutation	c.768G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379826
Start	36865739:36865739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191749029
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379826
Start	36865589:36865589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379826
Start	36879480:36879480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755030932
CDS Mutation	c.210G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379826
Start	36853467:36853467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755637337
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379826
Start	36879375:36879375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762750720
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379826
Start	36879408:36879408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779255458
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379826
Start	36848811:36848812(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1268dupG
AA Mutation	p.Ala424CysfsTer2(p.A424Cfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SMAD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379826
Start	36879641:36879641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>A
AA Mutation	p.Ala17Thr(p.A17T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379826
Start	36872658:36872658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670G>T
AA Mutation	p.Val224Phe(p.V224F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379826
Start	36879462:36879462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript