Variant #0001045879 (NC_000003.11:g.135871121G>T, NM_002718.4:c.*7113G>T (PPP2R3A))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.135871121G>T
DNA change (hg38) -
Published as MSL2(NM_018133.4):c.602C>A (p.S201*)
ISCN -
DB-ID MSL2_000016
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-07-08 13:22:38 +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     
PPP2R3A NM_002718.4 +?/. - c.*7113G>T r.(=) p.(=)
MSL2 NM_018133.3 +?/. - c.602C>A r.(?) p.(Ser201*)


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