Variant #0000977139 (NC_000006.11:g.29638166G>A, NM_001109809.2:c.*2111C>T (ZFP57))

Chromosome 6
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.29638166G>A
DNA change (hg38) -
Published as MOG(NM_002433.4):c.701G>A (p.(Arg234Lys))
ISCN -
DB-ID MOG_000048
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.*2111C>T r.(=) p.(=)
MOG NM_002433.4 ?/. - c.701G>A r.(?) p.(Arg234Lys)


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