Variant #0000716914 (NC_000001.10:g.156834553G>T, NM_002529.3:c.321G>T (NTRK1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.156834553G>T
DNA change (hg38) -
Published as NTRK1(NM_002529.3):c.321G>T (p.A107=)
ISCN -
DB-ID NTRK1_000242
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 2021-02-08 18:36:18 +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.321G>T r.(?) p.(Ala107=)
SH2D2A NM_003975.3 -?/. - c.-48053C>A r.(?) p.(=)
INSRR NM_014215.2 -?/. - c.-6140C>A r.(?) p.(=)


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