Colon Cancer: Gene >> ULK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19781967:19781967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2561G>A
AA Mutation	p.Cys854Tyr(p.C854Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19810392:19810392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1143C>A
AA Mutation	p.Phe381Leu(p.F381L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19816884:19816884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961T>G
AA Mutation	p.Leu321Val(p.L321V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19846835:19846835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>T
AA Mutation	p.Ser124Ile(p.S124I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19783707:19783707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2450C>T
AA Mutation	p.Thr817Met(p.T817M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19783740:19783740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2417T>C
AA Mutation	p.Ile806Thr(p.I806T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19801860:19801860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358C>T
AA Mutation	p.Ser453Phe(p.S453F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19783858:19783858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745490553
CDS Mutation	c.2299G>A
AA Mutation	p.Val767Met(p.V767M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19846807:19846807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399A>T
AA Mutation	p.Lys133Asn(p.K133N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19786083:19786083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2105C>T
AA Mutation	p.Pro702Leu(p.P702L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19804754:19804754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779492829
CDS Mutation	c.1234C>T
AA Mutation	p.Arg412Cys(p.R412C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19838527:19838527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761G>T
AA Mutation	p.Arg254Ile(p.R254I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19781039:19781039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2705C>T
AA Mutation	p.Ala902Val(p.A902V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19780599:19780599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2789T>G
AA Mutation	p.Phe930Cys(p.F930C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19796177:19796177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760552512
CDS Mutation	c.1915C>T
AA Mutation	p.Pro639Ser(p.P639S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19781057:19781057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780072901
CDS Mutation	c.2687C>T
AA Mutation	p.Ala896Val(p.A896V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361658
Start	19796133:19796133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1959G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361658
Start	19783706:19783706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146928634
CDS Mutation	c.2451G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361658
Start	19781905:19781905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2623C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000361658
Start	19826140:19826140(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.834delA
AA Mutation	p.Lys278AsnfsTer130(p.K278Nfs*130)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361658
Start	19826176:19826176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.798delT
AA Mutation	p.Phe266LeufsTer11(p.F266Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000361658
Start	19797668:19797668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1537C>T
AA Mutation	p.Gln513Ter(p.Q513*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000361658
Start	19826139:19826140(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.834dupA
AA Mutation	p.Ser279IlefsTer64(p.S279Ifs*64)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361658
Start	19797665:19797666(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1539dupA
AA Mutation	p.Ala514SerfsTer12(p.A514Sfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000361658
Start	19843224:19843224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000361658
Start	19797684:19797684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1523-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ULK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19846749:19846749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374423970
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Cys(p.R153C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19804808:19804808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1180C>T
AA Mutation	p.Pro394Ser(p.P394S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361658
Start	19816805:19816805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040C>A
AA Mutation	p.Ser347Tyr(p.S347Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361658
Start	19783781:19783781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144733183
CDS Mutation	c.2376C>T
Mutation Classification	Silent
Feature Type	Transcript