Variant #0000528161 (NC_000006.11:g.29638101T>C, NM_001109809.2:c.*2176A>G (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.29638101T>C
DNA change (hg38) g.29670324T>C
Published as MOG(NM_002433.4):c.636T>C (p.(Phe212=))
ISCN -
DB-ID MOG_000008
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) 0.00289 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZFP57 NM_001109809.2 -?/. - c.*2176A>G r.(=) p.(=)
MOG NM_002433.4 -?/. - c.636T>C r.(?) p.(Phe212=)


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