Variant #0000332404 (NC_000008.10:g.144999446G>A, NM_000445.3:c.4732C>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.144999446G>A
DNA change (hg38) g.143925278G>A
Published as PLEC(NM_000445.3):c.4732C>T (p.(Arg1578Cys)), PLEC(NM_201380.3):c.5062C>T (p.R1688C), PLEC(NM_201380.4):c.5062C>T (p.R1688C)
ISCN -
DB-ID PLEC_000149 See all 8 reported entries
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) 0.00244 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEC NM_000445.3 ?/. - c.4732C>T r.(?) p.(Arg1578Cys)
PLEC NM_201384.1 ?/. - c.4651C>T r.(?) p.(Arg1551Cys)


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