Variant #0000610193 (NC_000006.11:g.161127501A>G, NM_000301.3:c.112A>G (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.161127501A>G
DNA change (hg38) g.160706469A>G
Published as PLG(NM_000301.3):c.112A>G (p.K38E), PLG(NM_000301.5):c.112A>G (p.K38E)
ISCN -
DB-ID PLG_000017 See all 5 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) 0.00289 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLG NM_000301.3 ?/. - c.112A>G r.(?) p.(Lys38Glu)


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