Specific Information of Variant: 21-43658154-C-T
General Information
Variant ID 21-43658154-C-T
Genome Position chr21:43658154
ClinVar .

Related Small Proteins
SmProt IDLengthStart CodonStrandBlocksConsequence
SPROHSA77998 57AGG-43658073-43658247Non-Synonymous p.V32M
SPROHSA234589 57ATT-43656679-43656737,43658060-43658176Non-Synonymous p.R8H
SPROHSA235490 74ATT-43656679-43656737,43658060-43658227Non-Synonymous p.R25H
SPROHSA273594 53CTG-43658073-43658235Non-Synonymous p.V28M

Data sources
SourceAllele Count Allele Frequency
gnomAD3830080.57966
1KGP331780.63458
TOPMed724330.57684
GAsP25420.731
NyuWa44740.74592
Ribosome profilingSRR5382423; SRR6053333; SRR3680966; SRR3680967; SRR618771; SRR618773

5'UTR Effect
Variant Type uAUG_gained
Gene HSF2BP
Context TCACGCC
Kozak Strength Moderate
Effect out-of-frame_oORF
Distance to CDS 58
Distance to Alt Stop .

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