Variant #0000571863 (NC_000022.10:g.36661354C>T, NM_145343.2:c.520C>T (APOL1))

Chromosome 22
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.36661354C>T
DNA change (hg38) g.36265308C>T
Published as APOL1(NM_003661.3):c.472C>T (p.(Leu158Phe)), APOL1(NM_145343.2):c.520C>T (p.L174F)
ISCN -
DB-ID APOL1_000021 See all 3 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) 0.00195 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOL1 NM_145343.2 -/. - c.520C>T r.(?) p.(Leu174Phe)


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