Variant #0000256431 (NC_000023.10:g.22291839A>G, NM_182699.3:c.-726336A>G (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.22291839A>G
DNA change (hg38) g.22273722A>G
Published as ZNF645(NM_152577.3):c.731A>G (p.Q244R)
ISCN -
DB-ID ZNF645_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) 3.0E-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 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.731A>G r.(?) p.(Gln244Arg)
DDX53 NM_182699.3 ?/. - c.-726336A>G r.(?) p.(=)


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