Variant #0000559296 (NC_000016.9:g.81927404G>A, NC_000016.9(NM_002661.3):c.1072+5G>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.81927404G>A
DNA change (hg38) g.81893799G>A
Published as PLCG2(NM_002661.3):c.1072+5G>A (p.?), PLCG2(NM_002661.5):c.1072+5G>A
ISCN -
DB-ID PLCG2_000083 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLCG2 NM_002661.3 ?/. - c.1072+5G>A r.spl? p.?


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