Colon Cancer: Gene >> NUMBL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252891
Start	40681012:40681012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>T
AA Mutation	p.Pro149Ser(p.P149S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252891
Start	40686992:40686992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760792387
CDS Mutation	c.28G>A
AA Mutation	p.Gly10Arg(p.G10R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252891
Start	40681033:40681033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424G>A
AA Mutation	p.Glu142Lys(p.E142K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252891
Start	40667941:40667941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746765421
CDS Mutation	c.1357G>T
AA Mutation	p.Val453Leu(p.V453L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252891
Start	40673514:40673514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866C>T
AA Mutation	p.Ala289Val(p.A289V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252891
Start	40667553:40667553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142060332
CDS Mutation	c.1745C>T
AA Mutation	p.Ala582Val(p.A582V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252891
Start	40667787:40667787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202221260
CDS Mutation	c.1511G>A
AA Mutation	p.Arg504Gln(p.R504Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000252891
Start	40681045:40681045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774749633
CDS Mutation	c.412G>A
AA Mutation	p.Asp138Asn(p.D138N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000252891
Start	40667632:40667632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1666C>T
AA Mutation	p.Arg556Cys(p.R556C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252891
Start	40673537:40673537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.843G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252891
Start	40681046:40681046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112715509
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000252891
Start	40668018:40668020(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1278_1280delCCA
AA Mutation	p.Gln446del(p.Q446del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NUMBL

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252891
Start	40668116:40668116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182C>A
Mutation Classification	Silent
Feature Type	Transcript