Variant #0000552905 (NC_000014.8:g.68252669G>A, NM_015346.3:c.3210C>T (ZFYVE26))

Chromosome 14
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.68252669G>A
DNA change (hg38) g.67785952G>A
Published as ZFYVE26(NM_015346.3):c.3210C>T (p.P1070=)
ISCN -
DB-ID ZFYVE26_000077
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) 0.00482 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-05 15:18:07 +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.3210C>T r.(?) p.(Pro1070=)


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