Colon Cancer: Gene >> NTRK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000524377
Start	156864751:156864751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs578095133
CDS Mutation	c.311G>A
AA Mutation	p.Arg104His(p.R104H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000524377
Start	156880026:156880026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761967383
CDS Mutation	c.2074C>T
AA Mutation	p.Arg692Cys(p.R692C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000524377
Start	156873803:156873803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139875058
CDS Mutation	c.1021G>A
AA Mutation	p.Val341Met(p.V341M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000524377
Start	156880041:156880041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2089G>C
AA Mutation	p.Glu697Gln(p.E697Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000524377
Start	156864760:156864760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540521894
CDS Mutation	c.320C>T
AA Mutation	p.Ala107Val(p.A107V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000524377
Start	156879333:156879333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2017A>G
AA Mutation	p.Arg673Gly(p.R673G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000524377
Start	156876206:156876206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1628T>G
AA Mutation	p.Val543Gly(p.V543G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000524377
Start	156881569:156881569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2318G>A
AA Mutation	p.Ser773Asn(p.S773N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000524377
Start	156875547:156875547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382G>T
AA Mutation	p.Gly461Val(p.G461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524377
Start	156876096:156876096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524377
Start	156871722:156871722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524377
Start	156873658:156873658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749993335
CDS Mutation	c.876G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524377
Start	156873880:156873880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1098C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000524377
Start	156881514:156881514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2263G>T
AA Mutation	p.Glu755Ter(p.E755*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NTRK1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524377
Start	156864755:156864755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs6340
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript