Variant #0000307722 (NC_000022.10:g.50886032G>A, NM_002972.2:c.5370C>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.50886032G>A
DNA change (hg38) g.50447603G>A
Published as SBF1(NM_002972.3):c.5370C>T (p.Y1790=), SBF1(NM_002972.4):c.5370C>T (p.Y1790=)
ISCN -
DB-ID SBF1_000012 See all 3 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) 0.00022 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SBF1 NM_002972.2 -?/. - c.5370C>T r.(?) p.(Tyr1790=)
PPP6R2 NM_014678.4 -?/. - c.*3356G>A r.(=) p.(=)


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