Variant #0000329113 (NC_000022.10:g.50885758A>G, NM_002972.2:c.5576T>C (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.50885758A>G
DNA change (hg38) g.50447329A>G
Published as SBF1(NM_002972.2):c.5576T>C (p.(Phe1859Ser))
ISCN -
DB-ID SBF1_000005
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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.5576T>C r.(?) p.(Phe1859Ser)
PPP6R2 NM_014678.4 ?/. - c.*3082A>G r.(=) p.(=)


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