Variant #0000566808 (NC_000019.9:g.30936560G>C, NM_014717.1:c.2091G>C (ZNF536))

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.30936560G>C
DNA change (hg38) g.30445653G>C
Published as ZNF536(NM_014717.1):c.2091G>C (p.(Glu697Asp)), ZNF536(NM_014717.3):c.2091G>C (p.E697D)
ISCN -
DB-ID ZNF536_000004 See all 2 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) 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 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF536 NM_014717.1 ?/. - c.2091G>C r.(?) p.(Glu697Asp)


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