Variant #0001057237 (NC_000022.10:g.50903295G>A, NM_002972.2:c.1384C>T (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.50903295G>A
DNA change (hg38) -
Published as SBF1(NM_002972.4):c.1384C>T (p.(Arg462Cys))
ISCN -
DB-ID PPP6R2_000125
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) 4.0E-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 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.1384C>T r.(?) p.(Arg462Cys)
PPP6R2 NM_014678.4 ?/. - c.*20619G>A r.(=) p.(=)


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