Variant #0000576686 (NC_000023.10:g.54011401C>T, NM_015107.2:c.2389G>A (PHF8))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54011401C>T
DNA change (hg38) g.53984968C>T
Published as PHF8(NM_015107.2):c.2389G>A (p.A797T)
ISCN -
DB-ID PHF8_000036
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) 3.0E-5 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 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF8 NM_001184896.1 -?/. - c.2497G>A r.(?) p.(Ala833Thr)
PHF8 NM_015107.2 -?/. - c.2389G>A r.(?) p.(Ala797Thr)


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