Variant #0000552917 (NC_000014.8:g.68270912_68270913del, NM_015346.3:c.1343_1344del (ZFYVE26))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.68270912_68270913del
DNA change (hg38) g.67804195_67804196del
Published as ZFYVE26(NM_015346.3):c.1343_1344delTC (p.L448Pfs*31)
ISCN -
DB-ID ZFYVE26_000084
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 2020-07-05 15:18:18 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZFYVE26 NM_015346.3 +/. - c.1343_1344del r.(?) p.(Leu448ProfsTer31)


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