Variant #0000718728 (NC_000002.11:g.27600471G>A, NM_144631.5:c.1567C>T (ZNF513))

Chromosome 2
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.27600471G>A
DNA change (hg38) -
Published as ZNF513(NM_144631.5):c.1567C>T (p.R523W)
ISCN -
DB-ID PPM1G_000014
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) 1.0E-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 2021-02-08 18:36:18 +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     
SNX17 NM_014748.3 ?/. - c.*885G>A r.(=) p.(=)
ZNF513 NM_144631.5 ?/. - c.1567C>T r.(?) p.(Arg523Trp)
PPM1G NM_177983.2 ?/. - c.*3995C>T r.(=) p.(=)


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