Variant #0001040326 (NC_000015.9:g.41106277A>C, NC_000015.9(NM_001077268.1):c.1337+9A>C (ZFYVE19))

Chromosome 15
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.41106277A>C
DNA change (hg38) -
Published as ZFYVE19(NM_001077268.2):c.1337+9A>C
ISCN -
DB-ID DNAJC17_000011
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) 0.0001 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     
ZFYVE19 NM_001077268.1 -?/. - c.1337+9A>C r.(=) p.(=)
PPP1R14D NM_017726.7 -?/. - c.*1617T>G r.(=) p.(=)
DNAJC17 NM_018163.2 -?/. - c.-6633T>G r.(?) p.(=)


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