Variant #0000854252 (NC_000015.9:g.91491410G>A, NM_018671.3:c.1634G>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.91491410G>A
DNA change (hg38) -
Published as UNC45A(NM_001039675.1):c.1589G>A (p.R530H)
ISCN -
DB-ID HDDC3_000004
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) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
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.1634G>A r.(?) p.(Arg545His)
HDDC3 NM_198527.2 ?/. - c.-15640C>T r.(?) p.(=)


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