Variant #0000543971 (NC_000011.9:g.45955752T>C, PHF21A(NM_001101802.1):c.1810A>G)

Chromosome 11
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.45955752T>C
DNA change (hg38) g.45934201T>C
Published as PHF21A(NM_001101802.1):c.1810A>G (p.I604V), PHF21A(NM_001101802.3):c.1810A>G (p.I604V)
ISCN -
DB-ID PHF21A_000001 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) 0.00144 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF21A NM_001101802.1 ?/. - c.1810A>G r.(?) p.(Ile604Val)