Variant #0000892443 (NC_000015.9:g.91493412C>T, NM_018671.3:c.2102C>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.91493412C>T
DNA change (hg38) -
Published as UNC45A(NM_018671.5):c.2102C>T (p.(Thr701Met), p.T701M)
ISCN -
DB-ID HDDC3_000006 See all 2 reported entries
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) 5.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UNC45A NM_018671.3 ?/. - c.2102C>T r.(?) p.(Thr701Met)
RCCD1 NM_033544.2 ?/. - c.-4974C>T r.(?) p.(=)
HDDC3 NM_198527.2 ?/. - c.-17642G>A r.(?) p.(=)


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