Variant #0000519201 (NC_000003.11:g.38049265T>C, NM_001130964.1:c.2333A>G (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.38049265T>C
DNA change (hg38) g.38007774T>C
Published as PLCD1(NM_001130964.1):c.2333A>G (p.*778Wext*10)
ISCN -
DB-ID PLCD1_000004
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_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 2020-06-12 16:27:35 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLCD1 NM_001130964.1 +/. - c.2333A>G r.(?) p.(Ter778TrpextTer10)
VILL NM_015873.3 +/. - c.*719T>C r.(=) p.(=)


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