Variant #0001031369 (NC_000001.10:g.156834152C>T, NM_002529.3:c.219C>T (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.156834152C>T
DNA change (hg38) -
Published as NTRK1(NM_002529.3):c.219C>T (p.I73=), NTRK1(NM_002529.4):c.219C>T (p.(Ile73=))
ISCN -
DB-ID NTRK1_000216 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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NTRK1 NM_002529.3 ?/. - c.219C>T r.(?) p.(Ile73=)
SH2D2A NM_003975.3 ?/. - c.-47652G>A r.(?) p.(=)
INSRR NM_014215.2 ?/. - c.-5739G>A r.(?) p.(=)


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