Variant #0000608338 (NC_000003.11:g.135871126_135871136del, NM_002718.4:c.*7118_*7128del (PPP2R3A))

Chromosome 3
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.135871126_135871136del
DNA change (hg38) g.136152284_136152294del
Published as MSL2(NM_018133.4):c.590_600delATAATGGGCTT (p.Y197Ffs*4)
ISCN -
DB-ID MSL2_000005
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-15 15:52:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP2R3A NM_002718.4 ?/. - c.*7118_*7128del r.(=) p.(=)
MSL2 NM_018133.3 ?/. - c.590_600del r.(?) p.(Tyr197PhefsTer4)


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