Variant #0000966643 (NC_000011.9:g.9878045C>T, NM_030962.3:c.2323G>A (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.9878045C>T
DNA change (hg38) -
Published as SBF2(NM_030962.3):c.2323G>A (p.G775S), SBF2(NM_030962.4):c.2323G>A (p.G775S)
ISCN -
DB-ID SBF2_000037 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) 0.00318 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SBF2 NM_030962.3 -?/. - c.2323G>A r.(?) p.(Gly775Ser)


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