Variant #0000295295 (NC_000011.9:g.9801925T>G, NM_030962.3:c.*40A>C (SBF2))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.9801925T>G
DNA change (hg38) g.9780378T>G
Published as SBF2(NM_030962.4):c.*40A>C, SBF2-AS1(NR_036485.1):n.211+21875T>G
ISCN -
DB-ID SBF2_000022
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) 0.30743 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     
SBF2 NM_030962.3 -/. - c.*40A>C r.(=) p.(=)
SBF2-AS1 NR_036485.1 -/. - n.211+21875T>G r.(?) -


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