Variant #0000720818 (NC_000006.11:g.29641440G>A, NM_001109809.2:c.448C>T (ZFP57))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29641440G>A
DNA change (hg38) -
Published as ZFP57(NM_001109809.5):c.448C>T (p.Q150*)
ISCN -
DB-ID MOG_000029
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
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     
ZFP57 NM_001109809.2 +/. - c.448C>T r.(?) p.(Gln150*)
MOG NM_002433.4 +/. - c.*2213G>A r.(=) p.(=)


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