Variant #0000862629 (NC_000011.9:g.64701295C>T, NM_006244.3:c.1473C>T (PPP2R5B))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.64701295C>T
DNA change (hg38) -
Published as PPP2R5B(NM_006244.4):c.1473C>T (p.A491=)
ISCN -
DB-ID C11orf85_000001
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) 0.00408 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:51:19 +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     
C11orf85 NM_001037225.1 -?/. - c.*4752G>A r.(=) p.(=)
PPP2R5B NM_006244.3 -?/. - c.1473C>T r.(?) p.(Ala491=)
GPHA2 NM_130769.3 -?/. - c.*950G>A r.(=) p.(=)


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