Variant #0000575303 (NC_000023.10:g.22291554C>T, NM_182699.3:c.-726621C>T (DDX53))

Chromosome X
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.22291554C>T
DNA change (hg38) g.22273437C>T
Published as ZNF645(NM_152577.3):c.446C>T (p.S149L)
ISCN -
DB-ID ZNF645_000011
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-01-04 13:20:35 +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.446C>T r.(?) p.(Ser149Leu)
DDX53 NM_182699.3 -?/. - c.-726621C>T r.(?) p.(=)


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