Variant #0001055262 (NC_000015.9:g.91489935C>T, NM_018671.3:c.1291C>T (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.91489935C>T
DNA change (hg38) -
Published as UNC45A(NM_018671.5):c.1291C>T (p.(Arg431Trp))
ISCN -
DB-ID HDDC3_000026
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) 0.00019 View details
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.1291C>T r.(?) p.(Arg431Trp)
HDDC3 NM_198527.2 ?/. - c.-14165G>A r.(?) p.(=)


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