Variant #0000333423 (NC_000023.10:g.22291647T>A, NM_182699.3:c.-726528T>A (DDX53))

Chromosome X
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.22291647T>A
DNA change (hg38) g.22273530T>A
Published as ZNF645(NM_152577.3):c.539T>A (p.(Ile180Asn))
ISCN -
DB-ID ZNF645_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) 0.00086 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF645 NM_152577.3 ?/. - c.539T>A r.(?) p.(Ile180Asn)
DDX53 NM_182699.3 ?/. - c.-726528T>A r.(?) p.(=)


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