Variant #0000983785 (NC_000020.10:g.34542268G>A, NM_016436.4:c.*6719G>A (PHF20))

Chromosome 20
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.34542268G>A
DNA change (hg38) -
Published as SCAND1(NM_033630.3):c.-55-7C>T
ISCN -
DB-ID PHF20_000004
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) 0.00132 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 2024-04-19 20:27:30 +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     
PHF20 NM_016436.4 -?/. - c.*6719G>A r.(=) p.(=)
SCAND1 NM_016558.3 -?/. - c.-55-7C>T r.(=) p.(=)


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