Variant #0001045010 (NC_000001.10:g.156830736G>A, NM_002529.3:c.10G>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.156830736G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID NTRK1_000282
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs556840308
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00016 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-05-21 17:21:01 +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.10G>A r.(?) p.(Gly4Ser)


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