Colon Cancer: Gene >> TDP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335725
Start	89984542:89984542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34452707
CDS Mutation	c.911G>A
AA Mutation	p.Arg304Gln(p.R304Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335725
Start	90043115:90043115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772139596
CDS Mutation	c.1799C>T
AA Mutation	p.Thr600Met(p.T600M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335725
Start	89989043:89989043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1270G>T
AA Mutation	p.Gly424Trp(p.G424W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335725
Start	90019345:90019345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1571C>T
AA Mutation	p.Ala524Val(p.A524V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335725
Start	89993403:89993403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1461C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335725
Start	89963627:89963627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335725
Start	89984576:89984576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335725
Start	89963261:89963261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761583949
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000335725
Start	89984599:89984619(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.968_988delTCATCAGTTACTTGATGGCTT
AA Mutation	p.Leu323_Tyr330delinsHis(p.L323_Y330delinsH)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TDP1

No Mutation Annotation!