Colon Cancer: Gene >> YME1L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27147526:27147526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746220580
CDS Mutation	c.311G>A
AA Mutation	p.Arg104His(p.R104H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27134052:27134052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.933C>A
AA Mutation	p.Asn311Lys(p.N311K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27112016:27112016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2283T>G
AA Mutation	p.Ile761Met(p.I761M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27142417:27142417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571A>C
AA Mutation	p.Ser191Arg(p.S191R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27116234:27116234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2002G>A
AA Mutation	p.Asp668Asn(p.D668N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27123618:27123618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202A>G
AA Mutation	p.Tyr401Cys(p.Y401C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27120491:27120491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1526T>C
AA Mutation	p.Val509Ala(p.V509A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27122907:27122907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1340G>T
AA Mutation	p.Arg447Ile(p.R447I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326799
Start	27122960:27122960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1287G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326799
Start	27147645:27147645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141172987
CDS Mutation	c.192G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326799
Start	27117591:27117591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764613566
CDS Mutation	c.1875G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326799
Start	27134053:27134053(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.932delA
AA Mutation	p.Asn311ThrfsTer18(p.N311Tfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326799
Start	27145490:27145490(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.440delA
AA Mutation	p.Asn147ThrfsTer24(p.N147Tfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> YME1L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27154189:27154189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22G>A
AA Mutation	p.Val8Met(p.V8M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326799
Start	27117620:27117620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200047558
CDS Mutation	c.1846A>G
AA Mutation	p.Ile616Val(p.I616V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326799
Start	27114548:27114548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201724223
CDS Mutation	c.2151C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326799
Start	27147606:27147606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753921603
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000326799
Start	27136387:27136387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.602-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript