Variant #0001041830 (NC_000017.10:g.39973458G>A, NC_000017.10(NM_021939.3):c.391+3G>A (FKBP10))

Chromosome 17
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.39973458G>A
DNA change (hg38) -
Published as FKBP10(NM_021939.4):c.391+3G>A
ISCN -
DB-ID FKBP10_000109
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_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     
LEPREL4 NM_006455.2 ?/. - c.-5291C>T r.(?) p.(=)
FKBP10 NM_021939.3 ?/. - c.391+3G>A r.spl? p.?


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