Genomic variant #0000350209

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.33960567T>C
DNA change (hg38) -
Published as ZSCAN20(NM_145238.3):c.2623T>C (p.Tyr875His)
ISCN -
DB-ID ZSCAN20_000002
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
ZSCAN20 NM_145238.3 ?/. - c.2623T>C VUS r.(?) p.(Tyr875His)