Variant #0000305900 (NC_000006.11:g.161137790G>A, NM_000301.3:c.782G>A (PLG))

Chromosome 6
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.161137790G>A
DNA change (hg38) g.160716758G>A
Published as PLG(NM_000301.3):c.782G>A (p.R261H), PLG(NM_000301.5):c.782G>A (p.(Arg261His))
ISCN -
DB-ID PLG_000004 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Recognized as participating in HAE-PLG in a Portugese family
Reference Journal: Dias de Castro 2024
ClinVar ID ClinVar-RCV005392468.1
dbSNP ID rs4252187
Origin CLASSIFICATION record
Segregation -
Frequency 0.0025
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0025 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-11-05 17:49:45 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLG NM_000301.3 ?/. 7 c.782G>A r.(?) p.(Arg261His)


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