Variant #0000858478 (NC_000002.11:g.27601738C>G, NM_144631.5:c.395G>C (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.27601738C>G
DNA change (hg38) -
Published as ZNF513(NM_144631.5):c.395G>C (p.C132S)
ISCN -
DB-ID PPM1G_000019
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) 0.0008 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 2022-05-09 15:51:19 +02:00 (CEST)
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.*2152C>G r.(=) p.(=)
ZNF513 NM_144631.5 ?/. - c.395G>C r.(?) p.(Cys132Ser)
PPM1G NM_177983.2 ?/. - c.*2728G>C r.(=) p.(=)


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