Variant #0000503849 (NC_000001.10:g.156849894T>G, NM_002529.3:c.2150T>G (NTRK1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.156849894T>G
DNA change (hg38) g.156880102T>G
Published as NTRK1(NM_002529.4):c.2150T>G (p.L717R)
ISCN -
DB-ID NTRK1_000035 See all 2 reported entries
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.2150T>G r.(?) p.(Leu717Arg)
SH2D2A NM_003975.3 +/. - c.-63394A>C r.(?) p.(=)
INSRR NM_014215.2 +/. - c.-21481A>C r.(?) p.(=)


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