Variant #0000653785 (NC_000001.10:g.156830911T>C, NM_002529.3:c.185T>C (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.156830911T>C
DNA change (hg38) g.156861119T>C
Published as NTRK1(NM_002529.3):c.185T>C (p.L62P)
ISCN -
DB-ID NTRK1_000238
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
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.185T>C r.(?) p.(Leu62Pro)
SH2D2A NM_003975.3 ?/. - c.-44411A>G r.(?) p.(=)
INSRR NM_014215.2 ?/. - c.-2498A>G r.(?) p.(=)


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