Variant #0000892442 (NC_000015.9:g.91483608C>T, NM_018671.3:c.592C>T (UNC45A))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.91483608C>T
DNA change (hg38) -
Published as UNC45A(NM_018671.5):c.592C>T (p.Q198*)
ISCN -
DB-ID HDDC3_000005
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.592C>T r.(?) p.(Gln198*)
HDDC3 NM_198527.2 +/. - c.-7838G>A r.(?) p.(=)


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