Variant #0001006250 (NC_000022.10:g.50905850G>A, NM_002972.2:c.466C>T (SBF1))

Chromosome 22
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.50905850G>A
DNA change (hg38) -
Published as SBF1(NM_002972.4):c.466C>T (p.H156Y)
ISCN -
DB-ID PPP6R2_000117
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) 0.00045 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:16:32 +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     
SBF1 NM_002972.2 -?/. - c.466C>T r.(?) p.(His156Tyr)
PPP6R2 NM_014678.4 -?/. - c.*23174G>A r.(=) p.(=)


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