Variant #0001053156 (NC_000008.10:g.145009010G>A, NM_000445.3:c.994C>T (PLEC))

Chromosome 8
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.145009010G>A
DNA change (hg38) -
Published as PLEC(NM_201384.3):c.913C>T (p.(Arg305Cys))
ISCN -
DB-ID PLEC_000897
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) 3.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEC NM_000445.3 ?/. - c.994C>T r.(?) p.(Arg332Cys)
PLEC NM_201384.1 ?/. - c.913C>T r.(?) p.(Arg305Cys)


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