Variant #0000948683 (NC_000006.11:g.29640855C>G, NM_001109809.2:c.1033G>C (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.29640855C>G
DNA change (hg38) -
Published as ZFP57(NM_001109809.2):c.1033G>C (p.(Ala345Pro)), ZFP57(NM_001109809.5):c.1033G>C (p.A345P)
ISCN -
DB-ID MOG_000012 See all 2 reported entries
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) 0.00155 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 2023-11-27 17:35:39 +01:00 (CET)
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.1033G>C r.(?) p.(Ala345Pro)
MOG NM_002433.4 -?/. - c.*1628C>G r.(=) p.(=)


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