Variant #0000295261 (NC_000022.10:g.50903683G>A, NM_002972.2:c.1164C>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.50903683G>A
DNA change (hg38) g.50465254G>A
Published as SBF1(NM_002972.4):c.1164C>T (p.V388=)
ISCN -
DB-ID SBF1_000042
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) 0.0001 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SBF1 NM_002972.2 -?/. - c.1164C>T r.(?) p.(Val388=)
PPP6R2 NM_014678.4 -?/. - c.*21007G>A r.(=) p.(=)


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