Colon Cancer: Gene >> NOMO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14876671:14876671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2524C>T
AA Mutation	p.Pro842Ser(p.P842S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14876490:14876490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2488G>A
AA Mutation	p.Val830Ile(p.V830I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14866616:14866616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731G>T
AA Mutation	p.Glu577Asp(p.E577D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14882623:14882623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3057G>T
AA Mutation	p.Lys1019Asn(p.K1019N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14875154:14875154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752783819
CDS Mutation	c.2173G>A
AA Mutation	p.Gly725Ser(p.G725S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000287667
Start	14882595:14882595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201720548
CDS Mutation	c.3029C>T
AA Mutation	p.Pro1010Leu(p.P1010L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14863059:14863059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754351680
CDS Mutation	c.1267G>A
AA Mutation	p.Val423Ile(p.V423I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14864692:14864692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1503C>A
AA Mutation	p.Phe501Leu(p.F501L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14889163:14889163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3392C>A
AA Mutation	p.Ser1131Tyr(p.S1131Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14875058:14875058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2077G>A
AA Mutation	p.Ala693Thr(p.A693T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14880061:14880061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2804T>G
AA Mutation	p.Phe935Cys(p.F935C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287667
Start	14875156:14875156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757182691
CDS Mutation	c.2175C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287667
Start	14857318:14857318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1065C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287667
Start	14886838:14886838(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3305delC
AA Mutation	p.Pro1102HisfsTer42(p.P1102Hfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287667
Start	14846592:14846593(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.419_420dupAG
AA Mutation	p.Pro141SerfsTer12(p.P141Sfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NOMO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14895559:14895559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3583C>T
AA Mutation	p.Arg1195Cys(p.R1195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14844759:14844759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387C>A
AA Mutation	p.Phe129Leu(p.F129L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287667
Start	14853996:14853996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.933C>A
AA Mutation	p.Phe311Leu(p.F311L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287667
Start	14882611:14882611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767325995
CDS Mutation	c.3045C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287667
Start	14864716:14864716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527C>A
Mutation Classification	Silent
Feature Type	Transcript