Variant #0000856709 (NC_000023.10:g.54012261T>C, NM_015107.2:c.2117A>G (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.54012261T>C
DNA change (hg38) -
Published as PHF8(NM_015107.2):c.2117A>G (p.Y706C)
ISCN -
DB-ID PHF8_000062
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) 1.0E-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 2022-05-09 15:47:41 +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     
PHF8 NM_001184896.1 ?/. - c.2225A>G r.(?) p.(Tyr742Cys)
PHF8 NM_015107.2 ?/. - c.2117A>G r.(?) p.(Tyr706Cys)


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