Variant #0000798851 (NC_000001.10:g.156846279C>T, NM_002529.3:c.1720C>T (NTRK1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.156846279C>T
DNA change (hg38) -
Published as NTRK1(NM_002529.3):c.1720C>T (p.R574C)
ISCN -
DB-ID NTRK1_000252
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NTRK1 NM_002529.3 ?/. - c.1720C>T r.(?) p.(Arg574Cys)
SH2D2A NM_003975.3 ?/. - c.-59779G>A r.(?) p.(=)
INSRR NM_014215.2 ?/. - c.-17866G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.