Variant #0001042502 (NC_000018.9:g.60230244A>G, NM_017742.4:c.1553A>G (ZCCHC2))

Chromosome 18
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.60230244A>G
DNA change (hg38) -
Published as ZCCHC2(NM_017742.6):c.1553A>G (p.(Asn518Ser))
ISCN -
DB-ID ZCCHC2_000005
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) 0.00129 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZCCHC2 NM_017742.4 ?/. - c.1553A>G r.(?) p.(Asn518Ser)


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