Colon Cancer: Gene >> SCYL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367770
Start	169862728:169862728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1025T>G
AA Mutation	p.Leu342Arg(p.L342R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367770
Start	169854805:169854805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634T>C
AA Mutation	p.Ile545Thr(p.I545T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367770
Start	169862740:169862740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013T>C
AA Mutation	p.Val338Ala(p.V338A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367770
Start	169854784:169854784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655C>A
AA Mutation	p.Pro552His(p.P552H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367770
Start	169878804:169878804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Cys(p.R61C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367770
Start	169854295:169854295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2144A>G
AA Mutation	p.Lys715Arg(p.K715R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367770
Start	169888789:169888789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.52T>C
AA Mutation	p.Phe18Leu(p.F18L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367770
Start	169862625:169862625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1128C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367770
Start	169854528:169854528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551344610
CDS Mutation	c.1911G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367770
Start	169854534:169854534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772742115
CDS Mutation	c.1905C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367770
Start	169854907:169854907(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1532delA
AA Mutation	p.Asn511IlefsTer68(p.N511Ifs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000367770
Start	169854844:169854844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595G>A
AA Mutation	p.Trp532Ter(p.W532*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SCYL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367770
Start	169855869:169855869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1401C>A
AA Mutation	p.Phe467Leu(p.F467L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367770
Start	169878804:169878804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Cys(p.R61C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript