Colon Cancer: Gene >> CTSA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000191018
Start	45898092:45898092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144407534
CDS Mutation	c.1342G>A
AA Mutation	p.Ala448Thr(p.A448T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000191018
Start	45892775:45892775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000191018
Start	45894063:45894063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767712946
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000191018
Start	45891697:45891697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000191018
Start	45892305:45892305(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755100318
CDS Mutation	c.342delC
AA Mutation	p.Tyr115IlefsTer5(p.Y115Ifs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000191018
Start	45892795:45892796(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.517_518delTT
AA Mutation	p.Phe173ProfsTer39(p.F173Pfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000191018
Start	45895029:45895029(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs777834472
CDS Mutation	c.990delC
AA Mutation	p.Cys331AlafsTer36(p.C331Afs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000191018
Start	45891718:45891718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150C>A
AA Mutation	p.Tyr50Ter(p.Y50*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000191018
Start	45892271:45892271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000191018
Start	45898366:45898366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1360-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CTSA

No Mutation Annotation!