Variant #0000999038 (NC_000011.9:g.45959765dup, NM_001101802.1:c.1553dup (PHF21A))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45959765dup
DNA change (hg38) -
Published as PHF21A(NM_001101802.3):c.1553dupC (p.L519Sfs*53), PHF21A(NM_016621.4):c.1415dupC (p.L473Sfs*53)
ISCN -
DB-ID PHF21A_000034 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +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     
PHF21A NM_001101802.1 +/. - c.1553dup r.(?) p.(Leu519Serfs*53)


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