Variant #0000543978 (NC_000011.9:g.45971756C>T, PHF21A(NM_001101802.1):c.1144+1G>A)

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.45971756C>T
DNA change (hg38) g.45950205C>T
Published as PHF21A(NM_016621.3):c.1147+1G>A (p.?)
ISCN -
DB-ID PHF21A_000018
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF21A NM_001101802.1 ?/. - c.1144+1G>A r.spl? p.?