ClinVar Miner

List of variants in gene combination AP4M1, TAF6 reported as likely benign for not provided

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_004722.4(AP4M1):c.*219G>T rs4134930 0.00848
NM_139315.3(TAF6):c.1722C>T (p.Thr574=) rs145939245 0.00509
NM_004722.4(AP4M1):c.*387C>T rs146348021 0.00325
NM_139315.3(TAF6):c.1396G>T (p.Ala466Ser) rs144875978 0.00147
NM_139315.3(TAF6):c.1770C>T (p.Thr590=) rs145591068 0.00050
NM_139315.3(TAF6):c.1620A>C (p.Val540=) rs144479010 0.00047
NM_139315.3(TAF6):c.1899G>A (p.Ser633=) rs143687621 0.00041
NM_139315.3(TAF6):c.1657-12C>T rs375667816 0.00038
NM_139315.3(TAF6):c.2031G>A (p.Pro677=) rs771230753 0.00020
NM_139315.3(TAF6):c.1338C>T (p.Asp446=) rs200398416 0.00009
NM_139315.3(TAF6):c.1707G>A (p.Ser569=) rs749294882 0.00006
NM_139315.3(TAF6):c.1710C>T (p.Pro570=) rs138356641 0.00006
NM_139315.3(TAF6):c.1344T>C (p.Tyr448=) rs565026490 0.00002
NM_139315.3(TAF6):c.1905G>A (p.Pro635=) rs185657098 0.00002
NM_139315.3(TAF6):c.1329C>T (p.Asp443=) rs775428705 0.00001
NM_139315.3(TAF6):c.1459-19T>C rs1205200117 0.00001
NM_139315.3(TAF6):c.1671C>T (p.Ser557=) rs370671506 0.00001
NM_139315.3(TAF6):c.1689A>G (p.Ser563=) rs768942294 0.00001
NM_139315.3(TAF6):c.1725C>T (p.Val575=) rs1299756204 0.00001
NM_139315.3(TAF6):c.1459-5C>T rs200377684
NM_139315.3(TAF6):c.1470G>A (p.Thr490=)
NM_139315.3(TAF6):c.1821C>A (p.Ile607=)

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