Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SKIL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170391139:170391139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1775G>T
AA Mutation	p.Arg592Ile(p.R592I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170390382:170390382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1589T>C
AA Mutation	p.Ile530Thr(p.I530T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170360716:170360716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.385G>A
AA Mutation	p.Val129Ile(p.V129I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170391075:170391075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1711C>T
AA Mutation	p.Leu571Phe(p.L571F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170391214:170391214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1850G>A
AA Mutation	p.Cys617Tyr(p.C617Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170390337:170390337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770563584
CDS Mutation	c.1544C>T
AA Mutation	p.Pro515Leu(p.P515L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259119
Start	170361108:170361108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259119
Start	170360819:170360820(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.488_489insTGCTGCTG
AA Mutation	p.Lys163AsnfsTer12(p.K163Nfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SKIL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170360815:170360815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484G>A
AA Mutation	p.Glu162Lys(p.E162K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170390351:170390351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1558G>T
AA Mutation	p.Asp520Tyr(p.D520Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170360337:170360337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6A>C
AA Mutation	p.Glu2Asp(p.E2D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259119
Start	170390231:170390231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438A>C
AA Mutation	p.Ile480Leu(p.I480L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259119
Start	170390356:170390356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259119
Start	170361348:170361348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017T>C
Mutation Classification	Silent
Feature Type	Transcript