Specific Information of Variant: 9-34336268-C-T
General Information
Variant ID 9-34336268-C-T
Genome Position chr9:34336268
ClinVar .

Related Small Proteins
SmProt IDLengthStart CodonStrandBlocksConsequence
SPROHSA202216 15ATG+34336235-34336283Synonymous p.H11H

Data sources
SourceAllele Count Allele Frequency
gnomAD31055420.73803
1KGP339540.78954
TOPMed933310.74327
GAsP31270.9
NyuWa56240.93765
Ribosome profilingSRR3575898; SRR4045276; SRR5047771; SRR5047772; SRR5227294; SRR5239056; SRR5239057; SRR618771; SRR618773

5'UTR Effect
Variant Type uAUG_gained
Gene NUDT2
Context CCACGGA
Effect uORF_created
Distance to CDS 226
Distance to Alt Stop .

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