Variant #0001043112 (NC_000019.9:g.50316002G>C, NC_000019.9(NM_025129.4):c.112-9C>G (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.50316002G>C
DNA change (hg38) -
Published as FUZ(NM_025129.5):c.112-9C>G
ISCN -
DB-ID AP2A1_000010
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) 3.0E-5 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 2025-05-05 21:14:00 +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     
AP2A1 NM_014203.2 -?/. - c.*5987G>C r.(=) p.(=)
FUZ NM_025129.4 -?/. - c.112-9C>G r.(=) p.(=)


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