Colon Cancer: Gene >> CTSC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88294292:88294292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1106C>A
AA Mutation	p.Pro369His(p.P369H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88309253:88309253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551C>T
AA Mutation	p.Ser184Phe(p.S184F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88312478:88312478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575727793
CDS Mutation	c.395G>A
AA Mutation	p.Arg132Gln(p.R132Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88312458:88312458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749103588
CDS Mutation	c.415G>A
AA Mutation	p.Gly139Arg(p.G139R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88300607:88300607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.680A>C
AA Mutation	p.Lys227Thr(p.K227T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88294505:88294505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.893G>A
AA Mutation	p.Cys298Tyr(p.C298Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88294439:88294439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.959C>A
AA Mutation	p.Ala320Asp(p.A320D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88309193:88309193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611G>A
AA Mutation	p.Arg204Lys(p.R204K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88294080:88294080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754353507
CDS Mutation	c.1318C>T
AA Mutation	p.Arg440Trp(p.R440W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88300556:88300556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370851747
CDS Mutation	c.731A>G
AA Mutation	p.Asn244Ser(p.N244S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227266
Start	88300621:88300621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147642061
CDS Mutation	c.666T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227266
Start	88294105:88294105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1293C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227266
Start	88335066:88335066(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs774553369
CDS Mutation	c.189delA
AA Mutation	p.Val64Ter(p.V64*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000227266
Start	88300539:88300539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Ter(p.R250*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000227266
Start	88312548:88312548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>T
AA Mutation	p.Glu109Ter(p.E109*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227266
Start	88312496:88312497(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.376dupG
AA Mutation	p.Val126GlyfsTer3(p.V126Gfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227266
Start	88294117:88294118(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1280dupA
AA Mutation	p.Asn427LysfsTer9(p.N427Kfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227266
Start	88294495:88294496(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.902_903insT
AA Mutation	p.Phe302LeufsTer27(p.F302Lfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CTSC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227266
Start	88312413:88312413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.460G>A
AA Mutation	p.Ala154Thr(p.A154T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227266
Start	88334940:88334940(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.315delT
AA Mutation	p.Phe105LeufsTer10(p.F105Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript