ClinVar Miner

List of variants in gene HOXB13 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_006361.6(HOXB13):c.832G>T (p.Val278Leu) rs200997384 0.00008
NM_006361.6(HOXB13):c.140A>G (p.Asn47Ser) rs748333323 0.00006
NM_006361.6(HOXB13):c.216G>T (p.Gly72=) rs769145488
NM_006361.6(HOXB13):c.327C>A (p.Tyr109Ter) rs749101324
NM_006361.6(HOXB13):c.526G>C (p.Gly176Arg) rs747003841
NM_006361.6(HOXB13):c.543G>T (p.Gln181His) rs1597933867
NM_006361.6(HOXB13):c.587del (p.Lys196fs) rs771483373

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