Mutation

Primary Site >> Stomach Cancer

Gene >> NTRK3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88032881:88032881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1561C>A
AA Mutation	p.His521Asn(p.H521N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88137437:88137437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589C>T
AA Mutation	p.Leu197Phe(p.L197F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88183469:88183469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344T>C
AA Mutation	p.Leu115Pro(p.L115P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	87877084:87877084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773244598
CDS Mutation	c.2371C>T
AA Mutation	p.Arg791Trp(p.R791W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88137424:88137424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142726068
CDS Mutation	c.602G>A
AA Mutation	p.Arg201His(p.R201H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88032973:88032973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761822626
CDS Mutation	c.1469C>T
AA Mutation	p.Thr490Met(p.T490M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88135302:88135302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003T>C
AA Mutation	p.Trp335Arg(p.W335R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88183463:88183463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350G>C
AA Mutation	p.Ser117Thr(p.S117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	87877095:87877095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370533197
CDS Mutation	c.2360G>A
AA Mutation	p.Arg787His(p.R787H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88137484:88137484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542A>G
AA Mutation	p.Lys181Arg(p.K181R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88135328:88135328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764882745
CDS Mutation	c.977G>A
AA Mutation	p.Arg326His(p.R326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88032986:88032986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752483865
CDS Mutation	c.1456C>A
AA Mutation	p.His486Asn(p.H486N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360948
Start	88135976:88135976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830A>G
AA Mutation	p.Asp277Gly(p.D277G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	87933116:87933116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1785G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	87929335:87929335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758757427
CDS Mutation	c.1989C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88135942:88135942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770041052
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88126341:88126341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1326C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88184269:88184269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758172793
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88256007:88256007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360948
Start	88136539:88136539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000360948
Start	88256104:88256104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50T>A
AA Mutation	p.Leu17Ter(p.L17*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000360948
Start	88137402:88137402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript