Variant #0000326136 (NC_000019.9:g.9453026A>T, NM_001172651.1:c.-34127A>T (ZNF177))

Chromosome 19
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.9453026A>T
DNA change (hg38) g.9342350A>T
Published as ZNF559(NM_001202406.1):c.1091A>T (p.(Asn364Ile))
ISCN -
DB-ID ZNF559_000002
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) 0.00013 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
ZNF559-ZNF177 NM_001172650.2 ?/. - c.-391+3768A>T r.(=) p.(=)
ZNF177 NM_001172651.1 ?/. - c.-34127A>T r.(?) p.(=)
ZNF559 NM_032497.2 ?/. - c.899A>T r.(?) p.(Asn300Ile)


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