Variant #0000300735 (NC_000011.9:g.45957234G>A, PHF21A(NM_001101802.1):c.1738C>T)

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45957234G>A
DNA change (hg38) g.45935683G>A
Published as PHF21A(NM_001101802.2):c.1738C>T (p.R580*), PHF21A(NM_001101802.3):c.1738C>T (p.R580*), PHF21A(NM_001352025.1):c.1741C>T (p.R581*)
ISCN -
DB-ID PHF21A_000002 See all 4 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF21A NM_001101802.1 +?/. - c.1738C>T r.(?) p.(Arg580Ter)