Colon Cancer: Gene >> NELL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	20927322:20927322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>T
AA Mutation	p.Glu258Asp(p.E258D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	21113594:21113594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306G>A
AA Mutation	p.Asp436Asn(p.D436N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	21534466:21534466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749886230
CDS Mutation	c.1738G>A
AA Mutation	p.Gly580Ser(p.G580S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357134
Start	20919252:20919252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677C>T
AA Mutation	p.Thr226Ile(p.T226I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	20937827:20937827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039C>T
AA Mutation	p.Arg347Trp(p.R347W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	20937822:20937822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1034G>T
AA Mutation	p.Gly345Val(p.G345V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	21370942:21370942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639G>A
AA Mutation	p.Glu547Lys(p.E547K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	20937808:20937808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020A>C
AA Mutation	p.Lys340Asn(p.K340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	21570785:21570785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777090665
CDS Mutation	c.2002C>T
AA Mutation	p.Arg668Trp(p.R668W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	20918235:20918235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657G>C
AA Mutation	p.Gln219His(p.Q219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	20885491:20885491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776294059
CDS Mutation	c.554G>A
AA Mutation	p.Gly185Glu(p.G185E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	20947410:20947410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61150458
CDS Mutation	c.1146G>T
AA Mutation	p.Glu382Asp(p.E382D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357134
Start	20928477:20928477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995G>A
AA Mutation	p.Arg332Gln(p.R332Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357134
Start	20783830:20783830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335G>T
AA Mutation	p.Ser112Ile(p.S112I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	20919267:20919267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>T
AA Mutation	p.Ser231Ile(p.S231I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	20928386:20928386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375631199
CDS Mutation	c.904G>A
AA Mutation	p.Val302Met(p.V302M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357134
Start	21229387:21229387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357134
Start	21229423:21229423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117696889
CDS Mutation	c.1518G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000357134
Start	20783751:20783751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.256G>T
AA Mutation	p.Glu86Ter(p.E86*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NELL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	21570791:21570791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2008G>T
AA Mutation	p.Ala670Ser(p.A670S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	21534478:21534478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201961389
CDS Mutation	c.1750G>A
AA Mutation	p.Asp584Asn(p.D584N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357134
Start	21229419:21229419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514A>G
AA Mutation	p.Lys505Arg(p.K505R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357134
Start	20847619:20847619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357134
Start	21229351:21229351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561513540
CDS Mutation	c.1446C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000357134
Start	20783814:20783814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766250780
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Ter(p.R107*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000357134
Start	20928480:20928480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000357134
Start	20885443:20885443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript