Variant #0000248602 (NC_000008.10:g.145011204A>C, NM_000445.3:c.459T>G (PLEC))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145011204A>C
DNA change (hg38) g.143937036A>C
Published as PLEC(NM_201380.3):c.789T>G (p.A263=), PLEC(NM_201380.4):c.789T>G (p.A263=)
ISCN -
DB-ID PLEC_000218 See all 3 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) 0.00234 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.459T>G r.(?) p.(Ala153=)
PLEC NM_201384.1 -/. - c.378T>G r.(?) p.(Ala126=)


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