Variant #0000503819 (NC_000001.10:g.156816335C>T, NM_002529.3:c.-14392C>T (NTRK1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.156816335C>T
DNA change (hg38) g.156846543C>T
Published as INSRR(NM_014215.3):c.1786G>A (p.V596I)
ISCN -
DB-ID NTRK1_000215
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) 0.00041 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.-14392C>T r.(?) p.(=)
SH2D2A NM_003975.3 -?/. - c.-29835G>A r.(?) p.(=)
INSRR NM_014215.2 -?/. - c.1786G>A r.(?) p.(Val596Ile)


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