Variant #0001056905 (NC_000020.10:g.44579206C>T, NM_022095.3:c.3218G>A (ZNF335))

Chromosome 20
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.44579206C>T
DNA change (hg38) -
Published as ZNF335(NM_022095.4):c.3218G>A (p.(Arg1073Gln))
ISCN -
DB-ID PCIF1_000017
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
ZNF335 NM_022095.3 ?/. - c.3218G>A r.(?) p.(Arg1073Gln)
PCIF1 NM_022104.3 ?/. - c.*2812C>T r.(=) p.(=)


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