ClinVar Miner

List of variants in gene HOXB13 reported as uncertain significance for Prostate cancer, hereditary, 9

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_006361.6(HOXB13):c.251G>A (p.Gly84Glu) rs138213197 0.00160
NM_006361.6(HOXB13):c.832G>T (p.Val278Leu) rs200997384 0.00013
NM_006361.6(HOXB13):c.761G>C (p.Ser254Thr) rs769938759 0.00009
NM_006361.6(HOXB13):c.140A>G (p.Asn47Ser) rs748333323 0.00007
NM_006361.6(HOXB13):c.177G>A (p.Pro59=) rs779780541 0.00004
NM_006361.6(HOXB13):c.122C>T (p.Thr41Met) rs199799743 0.00003
NM_006361.6(HOXB13):c.302C>T (p.Ala101Val) rs763448911 0.00003
NM_006361.6(HOXB13):c.499G>A (p.Asp167Asn) rs587780164 0.00003
NM_006361.6(HOXB13):c.629C>T (p.Ala210Val) rs758190709 0.00003
NM_006361.6(HOXB13):c.215G>T (p.Gly72Val) rs774579054 0.00002
NM_006361.6(HOXB13):c.129G>A (p.Met43Ile) rs2038240627 0.00001
NM_006361.6(HOXB13):c.182A>T (p.Lys61Met) rs568967699 0.00001
NM_006361.6(HOXB13):c.198C>A (p.Cys66Ter) rs754885900 0.00001
NM_006361.6(HOXB13):c.209C>T (p.Pro70Leu) rs750621041 0.00001
NM_006361.6(HOXB13):c.319G>C (p.Ala107Pro) rs747755369 0.00001
NM_006361.6(HOXB13):c.445G>A (p.Val149Met) rs1597934198 0.00001
NM_006361.6(HOXB13):c.457G>T (p.Gly153Cys) rs754280897 0.00001
NM_006361.6(HOXB13):c.543G>T (p.Gln181His) rs1597933867 0.00001
NM_006361.6(HOXB13):c.563A>G (p.Gln188Arg) rs779330626 0.00001
NM_006361.6(HOXB13):c.208C>T (p.Pro70Ser) rs370934116
NM_006361.6(HOXB13):c.216G>T (p.Gly72=) rs769145488
NM_006361.6(HOXB13):c.254G>A (p.Gly85Asp) rs778563157
NM_006361.6(HOXB13):c.263A>G (p.Tyr88Cys)
NM_006361.6(HOXB13):c.281G>A (p.Arg94Gln) rs756135357
NM_006361.6(HOXB13):c.299G>T (p.Cys100Phe) rs1555558641
NM_006361.6(HOXB13):c.307G>A (p.Ala103Thr)
NM_006361.6(HOXB13):c.308C>T (p.Ala103Val) rs760196832
NM_006361.6(HOXB13):c.327C>A (p.Tyr109Ter) rs749101324
NM_006361.6(HOXB13):c.366C>A (p.Ser122Arg) rs8556
NM_006361.6(HOXB13):c.401C>G (p.Pro134Arg) rs1597934280
NM_006361.6(HOXB13):c.452C>G (p.Thr151Ser) rs1555558604
NM_006361.6(HOXB13):c.473C>A (p.Pro158Gln) rs1555558598
NM_006361.6(HOXB13):c.498G>A (p.Val166=) rs775189167
NM_006361.6(HOXB13):c.526G>C (p.Gly176Arg) rs747003841
NM_006361.6(HOXB13):c.54G>T (p.Leu18Phe) rs1597935263
NM_006361.6(HOXB13):c.574G>T (p.Gly192Cys)
NM_006361.6(HOXB13):c.587del (p.Lys196fs) rs771483373
NM_006361.6(HOXB13):c.634G>C (p.Ala212Pro) rs145059285
NM_006361.6(HOXB13):c.647_650dup (p.Lys218fs) rs1567701164
NM_006361.6(HOXB13):c.64G>A (p.Gly22Arg) rs539706443
NM_006361.6(HOXB13):c.650G>A (p.Arg217His) rs749518336
NM_006361.6(HOXB13):c.773G>A (p.Arg258His) rs367732101
NM_006361.6(HOXB13):c.847A>G (p.Thr283Ala) rs1295926376

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