Colon Cancer: Gene >> NTRK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	87929229:87929229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2095G>A
AA Mutation	p.Gly699Ser(p.G699S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88127221:88127221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143617169
CDS Mutation	c.1234G>A
AA Mutation	p.Glu412Lys(p.E412K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	87929289:87929289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2035G>A
AA Mutation	p.Asp679Asn(p.D679N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88136599:88136599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633G>T
AA Mutation	p.Glu211Asp(p.E211D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88137420:88137420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.606G>T
AA Mutation	p.Met202Ile(p.M202I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88137445:88137445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581G>A
AA Mutation	p.Gly194Asp(p.G194D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88184282:88184282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374069724
CDS Mutation	c.266G>A
AA Mutation	p.Arg89His(p.R89H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88147341:88147341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546426782
CDS Mutation	c.458G>A
AA Mutation	p.Arg153Gln(p.R153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88256098:88256098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.56G>A
AA Mutation	p.Gly19Glu(p.G19E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	87933169:87933169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1732A>G
AA Mutation	p.Thr578Ala(p.T578A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88135358:88135358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201426743
CDS Mutation	c.947G>A
AA Mutation	p.Arg316His(p.R316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88184268:88184268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280C>A
AA Mutation	p.Leu94Ile(p.L94I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88126292:88126292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750055690
CDS Mutation	c.1375C>T
AA Mutation	p.Arg459Trp(p.R459W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88032937:88032937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1505T>G
AA Mutation	p.Val502Gly(p.V502G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	87880318:87880318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2286G>T
AA Mutation	p.Glu762Asp(p.E762D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88136484:88136484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748T>C
AA Mutation	p.Ser250Pro(p.S250P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88135358:88135358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.947G>T
AA Mutation	p.Arg316Leu(p.R316L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88147350:88147350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449T>C
AA Mutation	p.Leu150Pro(p.L150P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88136605:88136605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88136584:88136584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201894375
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88147364:88147364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88256010:88256010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88135171:88135171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1134C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000360948
Start	88137534:88137534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492C>A
AA Mutation	p.Cys164Ter(p.C164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000360948
Start	88126295:88126295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372C>T
AA Mutation	p.Arg458Ter(p.R458*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000360948
Start	87929292:87929292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2032C>T
AA Mutation	p.Arg678Ter(p.R678*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000360948
Start	87940754:87940754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1586-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000360948
Start	88032855:88032855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1585+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NTRK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	87929241:87929241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2083A>T
AA Mutation	p.Ile695Phe(p.I695F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88126285:88126285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1382A>C
AA Mutation	p.Lys461Thr(p.K461T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	87929242:87929242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2082G>T
AA Mutation	p.Lys694Asn(p.K694N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88032959:88032959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1483G>T
AA Mutation	p.Asp495Tyr(p.D495Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88135310:88135310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145157285
CDS Mutation	c.995C>T
AA Mutation	p.Thr332Met(p.T332M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88255914:88255914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000360948
Start	88136568:88136568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Ter(p.R222*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000360948
Start	87940754:87940754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1586-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript