Variant #0000304657 (NC_000001.10:g.156846287C>T, NM_002529.3:c.1728C>T (NTRK1))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.156846287C>T
DNA change (hg38) g.156876495C>T
Published as NTRK1(NM_002529.3):c.1728C>T (p.F576=)
ISCN -
DB-ID NTRK1_000187
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) 0.00168 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NTRK1 NM_002529.3 -/. - c.1728C>T r.(?) p.(Phe576=)
SH2D2A NM_003975.3 -/. - c.-59787G>A r.(?) p.(=)
INSRR NM_014215.2 -/. - c.-17874G>A r.(?) p.(=)


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