Variant #0001014567 (NC_000009.11:g.87325623C>A, NM_006180.3:c.500C>A (NTRK2))

Chromosome 9
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.87325623C>A
DNA change (hg38) -
Published as NTRK2(NM_001369532.1):c.500C>A (p.S167Y), NTRK2(NM_006180.4):c.500C>A (p.S167Y), NTRK2(NM_006180.6):c.500C>A (p.S167Y)
ISCN -
DB-ID NTRK2_000002 See all 3 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) 0.00098 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NTRK2 NM_006180.3 -/. - c.500C>A r.(?) p.(Ser167Tyr)


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