Variant #0000452952 (NC_000001.10:g.156834169T>A, NM_002529.3:c.236T>A (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.156834169T>A
DNA change (hg38) g.156864377T>A
Published as -
ISCN -
DB-ID NTRK1_000013
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs139140006
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-11-02 10:36:02 +01:00 (CET)
Date last edited 2019-01-19 15:40:28 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NTRK1 NM_002529.3 ?/. - c.236T>A r.(?) p.(Leu79Gln)


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