Colon Cancer: Gene >> CSN1S1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246891
Start	69942546:69942546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376905625
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246891
Start	69944971:69944971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524A>T
AA Mutation	p.Asn175Ile(p.N175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246891
Start	69944943:69944943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149927680
CDS Mutation	c.496G>A
AA Mutation	p.Asp166Asn(p.D166N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246891
Start	69936570:69936570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158G>T
AA Mutation	p.Arg53Ile(p.R53I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246891
Start	69942556:69942556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246891
Start	69944977:69944977(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.536delA
AA Mutation	p.Asn179IlefsTer16(p.N179Ifs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246891
Start	69941022:69941023(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.304_305insTATTACACCTG
AA Mutation	p.Gln102LeufsTer9(p.Q102Lfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000246891
Start	69936481:69936481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CSN1S1

No Mutation Annotation!