Colon Cancer: Gene >> SCYL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270176
Start	65538076:65538076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2141C>T
AA Mutation	p.Pro714Leu(p.P714L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270176
Start	65526268:65526268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520C>T
AA Mutation	p.Pro174Ser(p.P174S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270176
Start	65536305:65536305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377549319
CDS Mutation	c.1622C>T
AA Mutation	p.Ser541Leu(p.S541L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270176
Start	65535981:65535981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1415T>C
AA Mutation	p.Phe472Ser(p.F472S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270176
Start	65531663:65531663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766077898
CDS Mutation	c.1096C>T
AA Mutation	p.Arg366Cys(p.R366C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270176
Start	65526850:65526850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670G>A
AA Mutation	p.Ala224Thr(p.A224T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000270176
Start	65538466:65538466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370701660
CDS Mutation	c.2327G>A
AA Mutation	p.Arg776Gln(p.R776Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270176
Start	65525231:65525231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270176
Start	65538086:65538086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758250704
CDS Mutation	c.2151C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270176
Start	65525642:65525642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270176
Start	65536129:65536129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376376282
CDS Mutation	c.1563C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270176
Start	65526220:65526220(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.476delG
AA Mutation	p.Gly159AlafsTer110(p.G159Afs*110)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270176
Start	65537001:65537001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1836delC
AA Mutation	p.Thr613ProfsTer60(p.T613Pfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SCYL1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270176
Start	65525956:65525956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000270176
Start	65535226:65535226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1231-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript