Variant #0000255925 (NC_000011.9:g.45948366del, PHF21A(NM_001101802.1):c.*7154del)

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.45948366del
DNA change (hg38) g.45926815del
Published as LARGE2(NM_152312.4):c.1269delA (p.E423Dfs*35)
ISCN -
DB-ID GYLTL1B_000004
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-30 13:18:24 +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.*7154del r.(?) p.(=)
GYLTL1B NM_152312.3 ?/. - c.1269del r.(?) p.(Glu423AspfsTer35)