Variant #0000515549 (NC_000002.11:g.27600972T>C, NM_144631.5:c.1066A>G (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.27600972T>C
DNA change (hg38) g.27378105T>C
Published as ZNF513(NM_144631.5):c.1066A>G (p.S356G)
ISCN -
DB-ID PPM1G_000005
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) 5.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.*1386T>C r.(=) p.(=)
ZNF513 NM_144631.5 -?/. - c.1066A>G r.(?) p.(Ser356Gly)
PPM1G NM_177983.2 -?/. - c.*3494A>G r.(=) p.(=)


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