Variant #0000961186 (NC_000001.10:g.91406272C>T, NM_201269.2:c.639G>A (ZNF644))

Chromosome 1
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.91406272C>T
DNA change (hg38) -
Published as ZNF644(NM_201269.2):c.639G>A (p.K213=), ZNF644(NM_201269.3):c.639G>A (p.K213=)
ISCN -
DB-ID ZNF644_000018 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) 0.00139 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +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     
ZNF644 NM_201269.2 -?/. - c.639G>A r.(?) p.(Lys213=)


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