Variant #0000503839 (NC_000001.10:g.156844703G>A, NM_002529.3:c.1257G>A (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.156844703G>A
DNA change (hg38) g.156874911G>A
Published as NTRK1(NM_002529.3):c.1257G>A (p.S419=)
ISCN -
DB-ID NTRK1_000226
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) 0.00056 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 2020-08-06 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.1257G>A r.(?) p.(Ser419=)
SH2D2A NM_003975.3 -?/. - c.-58203C>T r.(?) p.(=)
INSRR NM_014215.2 -?/. - c.-16290C>T r.(?) p.(=)


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