Variant #0000613789 (NC_000011.9:g.9809201_9809203del, NM_030962.3:c.5020_5022del (SBF2))

Chromosome 11
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.9809201_9809203del
DNA change (hg38) g.9787654_9787656del
Published as SBF2(NM_030962.3):c.5020_5022del (p.(Glu1674del)), SBF2(NM_030962.4):c.5020_5022delGAA (p.E1674del)
ISCN -
DB-ID SBF2_000025 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +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     
SBF2 NM_030962.3 -?/. - c.5020_5022del r.(?) p.(Glu1674del)
SBF2-AS1 NR_036485.1 -?/. - n.212-20194_212-20192del r.(?) -


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