Variant #0000568029 (NC_000019.9:g.50308795G>T, NM_025129.4:c.*1613C>A (FUZ))

Chromosome 19
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.50308795G>T
DNA change (hg38) g.49805538G>T
Published as AP2A1(NM_014203.2):c.2496G>T (p.R832=)
ISCN -
DB-ID AP2A1_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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 10:49:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP2A1 NM_014203.2 -?/. - c.2496G>T r.(?) p.(Arg832=)
FUZ NM_025129.4 -?/. - c.*1613C>A r.(=) p.(=)


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