Variant #0000332682 (NC_000009.11:g.96439006_96439007insTGCCTCCACCACCCC, NM_005392.3:c.2963_2964insTGCCTCCACCACCCC (PHF2))

Chromosome 9
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.96439006_96439007insTGCCTCCACCACCCC
DNA change (hg38) g.93676724_93676725insTGCCTCCACCACCCC
Published as PHF2(NM_005392.3):c.2955_2956insACCACCCCTGCCTCC (p.?)
ISCN -
DB-ID PHF2_000002
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) 0.00696 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF2 NM_005392.3 ?/. - c.2963_2964insTGCCTCCACCACCCC r.(?) p.(Thr992_Thr996dup)


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