Colon Cancer: Gene >> DNASE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246949
Start	3657245:3657245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.608G>T
AA Mutation	p.Trp203Leu(p.W203L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000246949
Start	3656102:3656102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237G>T
AA Mutation	p.Gln79His(p.Q79H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246949
Start	3657754:3657754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148684969
CDS Mutation	c.739G>A
AA Mutation	p.Val247Ile(p.V247I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246949
Start	3656178:3656178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313G>A
AA Mutation	p.Val105Met(p.V105M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246949
Start	3655909:3655909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571444570
CDS Mutation	c.208G>A
AA Mutation	p.Val70Met(p.V70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246949
Start	3657075:3657075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770091885
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000246949
Start	3656637:3656637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DNASE1

No Mutation Annotation!