Variant #0000305537 (NC_000023.10:g.53966697G>A, NM_015107.2:c.2902C>T (PHF8))

Chromosome X
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.53966697G>A
DNA change (hg38) g.53940264G>A
Published as PHF8(NM_015107.2):c.2902C>T (p.R968C)
ISCN -
DB-ID PHF8_000011
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 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.3010C>T r.(?) p.(Arg1004Cys)
PHF8 NM_015107.2 ?/. - c.2902C>T r.(?) p.(Arg968Cys)


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