Variant #0000998735 (NC_000011.9:g.111613299G>A, NM_002716.4:c.1645C>T (PPP2R1B))

Chromosome 11
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.111613299G>A
DNA change (hg38) -
Published as PPP2R1B(NM_002716.4):c.1645C>T (p.(Arg549Cys))
ISCN -
DB-ID PPP2R1B_000004
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) 0.00013 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP2R1B NM_002716.4 ?/. - c.1645C>T r.(?) p.(Arg549Cys)
SIK2 NM_015191.1 ?/. - c.*18446G>A r.(=) p.(=)


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