Variant #0000993597 (NC_000003.11:g.38050599C>T, NM_001130964.1:c.1720G>A (PLCD1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.38050599C>T
DNA change (hg38) -
Published as PLCD1(NM_006225.3):c.1657G>A (p.(Ala553Thr))
ISCN -
DB-ID PLCD1_000018
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) 0.00019 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 2024-08-28 13:16:32 +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     
PLCD1 NM_001130964.1 +?/. - c.1720G>A r.(?) p.(Ala574Thr)
VILL NM_015873.3 +?/. - c.*2053C>T r.(=) p.(=)


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