Variant #0000515551 (NC_000002.11:g.27601160C>T, NM_144631.5:c.878G>A (ZNF513))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27601160C>T
DNA change (hg38) g.27378293C>T
Published as ZNF513(NM_144631.5):c.878G>A (p.R293Q), ZNF513(NM_144631.6):c.878G>A (p.R293Q)
ISCN -
DB-ID ZNF513_000011 See all 3 reported entries
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) 0.00131 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNX17 NM_014748.3 -/. - c.*1574C>T r.(=) p.(=)
ZNF513 NM_144631.5 -/. - c.878G>A r.(?) p.(Arg293Gln)
PPM1G NM_177983.2 -/. - c.*3306G>A r.(=) p.(=)


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