Variant #0000296938 (NC_000023.10:g.53966879C>T, NM_015107.2:c.2720G>A (PHF8))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53966879C>T
DNA change (hg38) g.53940446C>T
Published as PHF8(NM_001184896.1):c.2828G>A (p.(Arg943His)), PHF8(NM_015107.2):c.2720G>A (p.R907H), PHF8(NM_015107.3):c.2720G>A (p.R907H)
ISCN -
DB-ID PHF8_000012 See all 4 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) 0.00213 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF8 NM_001184896.1 -/. - c.2828G>A r.(?) p.(Arg943His)
PHF8 NM_015107.2 -/. - c.2720G>A r.(?) p.(Arg907His)


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