Variant #0001024793 (NC_000003.11:g.38051981del, NM_001130964.1:c.926del (PLCD1))

Chromosome 3
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.38051981del
DNA change (hg38) -
Published as PLCD1(NM_001130964.2):c.926delG (p.S309Tfs*33)
ISCN -
DB-ID PLCD1_000019
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLCD1 NM_001130964.1 +/. - c.926del r.(?) p.(Ser309Thrfs*33)
VILL NM_015873.3 +/. - c.*3435del r.(?) p.(=)


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