Variant #0000561439 (NC_000017.10:g.39969458G>A, NM_021939.3:c.172G>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.39969458G>A
DNA change (hg38) g.41813206G>A
Published as FKBP10(NM_021939.3):c.172G>A (p.(Glu58Lys))
ISCN -
DB-ID FKBP10_000073
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LEPREL4 NM_006455.2 ?/. - c.-1291C>T r.(?) p.(=)
FKBP10 NM_021939.3 ?/. - c.172G>A r.(?) p.(Glu58Lys)


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