Variant #0000983405 (NC_000019.9:g.3653524_3653525del, NM_012398.2:c.688_689del (PIP5K1C))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.3653524_3653525del
DNA change (hg38) -
Published as PIP5K1C(NM_012398.3):c.688_689del (p.(Gly230GlnfsTer114))
ISCN -
DB-ID PIP5K1C_000027
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
PIP5K1C NM_012398.2 ?/. - c.688_689del r.(?) p.(Gly230Glnfs*114)


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