Variant #0000559279 (NC_000016.9:g.81819751G>A, NM_002661.3:c.157G>A (PLCG2))

Chromosome 16
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.81819751G>A
DNA change (hg38) g.81786146G>A
Published as PLCG2(NM_002661.3):c.157G>A (p.A53T, p.(Ala53Thr)), PLCG2(NM_002661.5):c.157G>A (p.A53T)
ISCN -
DB-ID PLCG2_000070 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) 2.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
PLCG2 NM_002661.3 ?/. - c.157G>A r.(?) p.(Ala53Thr)


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