Variant #0001001808 (NC_000015.9:g.91496515C>T, NM_018671.3:c.2552C>T (UNC45A))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.91496515C>T
DNA change (hg38) -
Published as UNC45A(NM_018671.3):c.2552C>T (p.(Thr851Met))
ISCN -
DB-ID HDDC3_000017
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) 7.0E-5 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 2024-08-28 13:16:32 +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     
UNC45A NM_018671.3 -?/. - c.2552C>T r.(?) p.(Thr851Met)
RCCD1 NM_033544.2 -?/. - c.-1871C>T r.(?) p.(=)
HDDC3 NM_198527.2 -?/. - c.-20745G>A r.(?) p.(=)


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