Colon Cancer: Gene >> CSN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304954
Start	70249235:70249235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192474479
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Cys(p.R109C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304954
Start	70249196:70249196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs74750151
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Trp(p.R96W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304954
Start	70249054:70249054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
AA Mutation	p.Met48Ile(p.M48I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304954
Start	70249220:70249220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310C>A
AA Mutation	p.Pro104Thr(p.P104T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant;stop_lost
Transcription ID	ENST00000304954
Start	70249458:70249458(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.*3delA
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304954
Start	70249292:70249292(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.385delA
AA Mutation	p.Ile129Ter(p.I129*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000304954
Start	70249199:70249199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289C>T
AA Mutation	p.Gln97Ter(p.Q97*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304954
Start	70249269:70249270(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.365dupC
AA Mutation	p.Lys124GlufsTer5(p.K124Efs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CSN3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304954
Start	70249357:70249357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754067840
CDS Mutation	c.447A>G
Mutation Classification	Silent
Feature Type	Transcript