Variant #0000997038 (NC_000008.10:g.145003653C>T, NM_000445.3:c.3091G>A (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.145003653C>T
DNA change (hg38) -
Published as PLEC(NM_201384.1):c.3010G>A (p.(Val1004Met))
ISCN -
DB-ID PLEC_000374 See all 2 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) 0.00013 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEC NM_000445.3 ?/. - c.3091G>A r.(?) p.(Val1031Met)
PLEC NM_201384.1 ?/. - c.3010G>A r.(?) p.(Val1004Met)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.