Primary Site >> Liver Cancer

Gene >> NTRK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000323115
Start 84727789:84727789(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.989T>C
AA Mutation p.Ile330Thr(p.I330T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000323115
Start 84710683:84710683(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.475A>T
AA Mutation p.Ile159Phe(p.I159F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000323115
Start 84724306:84724306(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.803C>T
AA Mutation p.Ala268Val(p.A268V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000323115
Start 85020270:85020270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2189T>G
AA Mutation p.Phe730Cys(p.F730C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000323115
Start 85021261:85021261(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2293T>C
AA Mutation p.Cys765Arg(p.C765R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000323115
Start 84745026:84745026(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1249A>T
AA Mutation p.Ile417Phe(p.I417F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000323115
Start 84955331:84955331(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1938G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000323115
Start 85020319:85020319(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2238T>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000323115
Start 84745060:84745060(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1285delG
AA Mutation p.Glu429AsnfsTer10(p.E429Nfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript