Variant #0000311474 (NC_000002.11:g.27601724C>T, NM_144631.5:c.409G>A (ZNF513))

Chromosome 2
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.27601724C>T
DNA change (hg38) g.27378857C>T
Published as ZNF513(NM_144631.6):c.409G>A (p.G137R)
ISCN -
DB-ID ZNF513_000007
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) 4.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNX17 NM_014748.3 -?/. - c.*2138C>T r.(=) p.(=)
ZNF513 NM_144631.5 -?/. - c.409G>A r.(?) p.(Gly137Arg)
PPM1G NM_177983.2 -?/. - c.*2742G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.