Variant #0000924465 (NC_000006.11:g.29641216C>T, NM_001109809.2:c.672G>A (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.29641216C>T
DNA change (hg38) -
Published as ZFP57(NM_001109809.2):c.672G>A (p.(Met224Ile))
ISCN -
DB-ID MOG_000045
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZFP57 NM_001109809.2 ?/. - c.672G>A r.(?) p.(Met224Ile)
MOG NM_002433.4 ?/. - c.*1989C>T r.(=) p.(=)


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