Colon Cancer: Gene >> NTRK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	85020227:85020227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2146C>T
AA Mutation	p.Pro716Ser(p.P716S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	85020321:85020321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2240T>G
AA Mutation	p.Phe747Cys(p.F747C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84724293:84724293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790A>T
AA Mutation	p.Ile264Phe(p.I264F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84670789:84670789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41G>A
AA Mutation	p.Arg14Gln(p.R14Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84723658:84723658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669T>A
AA Mutation	p.Asp223Glu(p.D223E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84723627:84723627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638C>T
AA Mutation	p.Ser213Phe(p.S213F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84955302:84955302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200114699
CDS Mutation	c.1909G>A
AA Mutation	p.Val637Met(p.V637M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84955377:84955377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1984G>A
AA Mutation	p.Ala662Thr(p.A662T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84670845:84670845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>G
AA Mutation	p.Pro33Ala(p.P33A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84670788:84670788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40C>T
AA Mutation	p.Arg14Trp(p.R14W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84710654:84710654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446C>A
AA Mutation	p.Pro149Gln(p.P149Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84710719:84710719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511A>C
AA Mutation	p.Thr171Pro(p.T171P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84723699:84723699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.710C>T
AA Mutation	p.Ser237Phe(p.S237F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	85021277:85021277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201491838
CDS Mutation	c.2309G>A
AA Mutation	p.Arg770Gln(p.R770Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84934269:84934269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1693G>A
AA Mutation	p.Asp565Asn(p.D565N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84707855:84707855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781137734
CDS Mutation	c.371G>A
AA Mutation	p.Arg124Gln(p.R124Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323115
Start	84670904:84670904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323115
Start	84744989:84744989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769551088
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323115
Start	84955493:84955493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773274918
CDS Mutation	c.2100C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323115
Start	84702210:84702210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323115
Start	84745010:84745010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141562338
CDS Mutation	c.1233G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323115
Start	84955331:84955331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1938G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323115
Start	84723613:84723613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323115
Start	85020277:85020277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2196G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	inframe_insertion;splice_region_variant
Transcription ID	ENST00000323115
Start	84702419:84702420(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.359_359+1insTAGAAC
AA Mutation	p.Ile120_Asn121insArgThr(p.I120_N121insRT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NTRK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323115
Start	84724264:84724264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761A>G
AA Mutation	p.Asn254Ser(p.N254S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323115
Start	84948548:84948548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1803C>G
Mutation Classification	Silent
Feature Type	Transcript