Variant #0000861124 (NC_000008.10:g.145013572T>C, NC_000008.10(NM_000445.3):c.194-712A>G (PLEC))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145013572T>C
DNA change (hg38) -
Published as PLEC(NM_201384.1):c.58A>G (p.(Ser20Gly)), PLEC(NM_201384.2):c.58A>G (p.S20G)
ISCN -
DB-ID PLEC_000221 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) 0.00065 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEC NM_000445.3 -?/. - c.194-712A>G r.(=) p.(=)
PLEC NM_201384.1 -?/. - c.58A>G r.(?) p.(Ser20Gly)


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