Variant #0000890055 (NC_000011.9:g.64693374G>C, NM_006244.3:c.168G>C (PPP2R5B))

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.64693374G>C
DNA change (hg38) -
Published as PPP2R5B(NM_006244.3):c.168G>C (p.(Gln56His))
ISCN -
DB-ID GPHA2_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP2R5B NM_006244.3 ?/. - c.168G>C r.(?) p.(Gln56His)
GPHA2 NM_130769.3 ?/. - c.*8871C>G r.(=) p.(=)


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