Variant #0000860276 (NC_000006.11:g.29641329G>A, NM_001109809.2:c.559C>T (ZFP57))

Chromosome 6
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.29641329G>A
DNA change (hg38) -
Published as ZFP57(NM_001109809.2):c.559C>T (p.(Arg187Cys))
ISCN -
DB-ID ZFP57_000005 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) 0.05093 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZFP57 NM_001109809.2 -?/. - c.559C>T r.(?) p.(Arg187Cys)
MOG NM_002433.4 -?/. - c.*2102G>A r.(=) p.(=)


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