Variant #0000514053 (NC_000002.11:g.209200586_209200587del, NM_015040.3:c.4326_4327del (PIKFYVE))

Chromosome 2
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.209200586_209200587del
DNA change (hg38) g.208335862_208335863del
Published as PIKFYVE(NM_015040.3):c.4326_4327delAA (p.E1444Gfs*16)
ISCN -
DB-ID PIKFYVE_000029
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 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIKFYVE NM_015040.3 +/. - c.4326_4327del r.(?) p.(Glu1444GlyfsTer16)


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