Variant #0001057236 (NC_000022.10:g.50903253T>C, NM_002972.2:c.1426A>G (SBF1))

Chromosome 22
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.50903253T>C
DNA change (hg38) -
Published as SBF1(NM_002972.4):c.1426A>G (p.K476E, p.(Lys476Glu))
ISCN -
DB-ID PPP6R2_000037 See all 2 reported entries
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) 0.00055 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 2025-11-01 13:22:20 +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     
SBF1 NM_002972.2 ?/. - c.1426A>G r.(?) p.(Lys476Glu)
PPP6R2 NM_014678.4 ?/. - c.*20577T>C r.(=) p.(=)


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