Variant #0000931314 (NC_000022.10:g.50900372G>A, NC_000022.10(NM_002972.2):c.2569+4C>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.50900372G>A
DNA change (hg38) -
Published as SBF1(NM_002972.4):c.2569+4C>T
ISCN -
DB-ID SBF1_000033 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) 0.001 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-07-07 10:10:56 +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.2569+4C>T r.spl? p.?
PPP6R2 NM_014678.4 -?/. - c.*17696G>A r.(=) p.(=)


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