Variant #0000979581 (NC_000011.9:g.45955613del, NM_001101802.1:c.1955del (PHF21A))

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.45955613del
DNA change (hg38) -
Published as PHF21A(NM_001352027.3):c.1958del (p.(Pro653Leufs*104))
ISCN -
DB-ID GYLTL1B_000027
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
Date created 2024-04-19 20:27:30 +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.1955del r.(?) p.(Pro652Leufs*104)
GYLTL1B NM_152312.3 +?/. - c.*5217del r.(?) p.(=)


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