Variant #0000676610 (NC_000002.11:g.27601345C>A, NM_144631.5:c.788G>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.27601345C>A
DNA change (hg38) -
Published as ZNF513(NM_144631.5):c.788G>T (p.R263L)
ISCN -
DB-ID PPM1G_000013
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) 8.0E-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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNX17 NM_014748.3 ?/. - c.*1759C>A r.(=) p.(=)
ZNF513 NM_144631.5 ?/. - c.788G>T r.(?) p.(Arg263Leu)
PPM1G NM_177983.2 ?/. - c.*3121G>T r.(=) p.(=)


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