Variant #0000287988 (NC_000019.9:g.50312653C>T, NM_025129.4:c.672G>A (FUZ))

Chromosome 19
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.50312653C>T
DNA change (hg38) g.49809396C>T
Published as FUZ(NM_025129.4):c.672G>A (p.L224=)
ISCN -
DB-ID FUZ_000001
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) 0.11757 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 10:49:24 +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.*2638C>T r.(=) p.(=)
FUZ NM_025129.4 -/. - c.672G>A r.(?) p.(Leu224=)


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