Variant #0000528168 (NC_000006.11:g.29641007G>A, NM_001109809.2:c.881C>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.29641007G>A
DNA change (hg38) g.29673230G>A
Published as ZFP57(NM_001109809.2):c.881C>T (p.(Thr294Ile))
ISCN -
DB-ID MOG_000015
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 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 2022-05-09 15:51:19 +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.881C>T r.(?) p.(Thr294Ile)
MOG NM_002433.4 ?/. - c.*1780G>A r.(=) p.(=)


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