Colon Cancer: Gene >> ROR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64137458:64137458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572C>A
AA Mutation	p.Ser191Tyr(p.S191Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64177871:64177871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1830C>A
AA Mutation	p.Phe610Leu(p.F610L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64140243:64140243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761386607
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Cys(p.R249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64140219:64140219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371024298
CDS Mutation	c.721G>A
AA Mutation	p.Val241Ile(p.V241I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64178808:64178808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2767G>T
AA Mutation	p.Ala923Ser(p.A923S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64178829:64178829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778919689
CDS Mutation	c.2788G>A
AA Mutation	p.Glu930Lys(p.E930K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64178707:64178707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2666C>T
AA Mutation	p.Ser889Leu(p.S889L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64178167:64178167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2126A>C
AA Mutation	p.Gln709Pro(p.Q709P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64177809:64177809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374512783
CDS Mutation	c.1768G>A
AA Mutation	p.Gly590Arg(p.G590R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64049871:64049871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757219208
CDS Mutation	c.344G>A
AA Mutation	p.Arg115Gln(p.R115Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371079
Start	64049977:64049977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450T>G
AA Mutation	p.Phe150Leu(p.F150L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64177533:64177533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492G>A
AA Mutation	p.Asp498Asn(p.D498N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371079
Start	64177511:64177511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1470C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371079
Start	64178618:64178618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2577C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371079
Start	64178669:64178669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2628C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371079
Start	64177808:64177808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779609145
CDS Mutation	c.1767C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371079
Start	64140194:64140194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371079
Start	64178552:64178552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2511G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371079
Start	64049920:64049920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148616064
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371079
Start	64140146:64140146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ROR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64049719:64049719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192G>T
AA Mutation	p.Met64Ile(p.M64I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64177931:64177931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1890G>T
AA Mutation	p.Lys630Asn(p.K630N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64178048:64178048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2007C>A
AA Mutation	p.Phe669Leu(p.F669L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64177442:64177442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1401G>T
AA Mutation	p.Glu467Asp(p.E467D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64049876:64049876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199925889
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Trp(p.R117W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64178772:64178772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2731A>C
AA Mutation	p.Lys911Gln(p.K911Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371079
Start	64159023:64159023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1217A>G
AA Mutation	p.Tyr406Cys(p.Y406C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371079
Start	64178816:64178816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2775T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000371079
Start	64050687:64050687(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.458delC
AA Mutation	p.Pro153LeufsTer46(p.P153Lfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript