Variant #0001055260 (NC_000015.9:g.91483531C>A, NC_000015.9(NM_018671.3):c.520-5C>A (UNC45A))

Chromosome 15
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.91483531C>A
DNA change (hg38) -
Published as UNC45A(NM_018671.5):c.520-5C>A
ISCN -
DB-ID HDDC3_000024
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UNC45A NM_018671.3 ?/. - c.520-5C>A r.spl? p.?
HDDC3 NM_198527.2 ?/. - c.-7761G>T r.(?) p.(=)


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