ClinVar Miner

List of variants in gene ST14 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_021978.4(ST14):c.508G>A (p.Glu170Lys) rs150984123 0.00205
NM_021978.4(ST14):c.1470C>T (p.Ala490=) rs140209483 0.00071
NM_021978.4(ST14):c.2304C>T (p.Ile768=) rs201796684 0.00057
NM_021978.4(ST14):c.522C>T (p.Ala174=) rs116759881 0.00054
NM_021978.4(ST14):c.1807+7A>G rs182276812 0.00047
NM_021978.4(ST14):c.1314C>T (p.Thr438=) rs144099671 0.00026
NM_021978.4(ST14):c.1248C>T (p.Phe416=) rs138855512 0.00010
NM_021978.4(ST14):c.180C>T (p.Ala60=) rs373655320 0.00009
NM_021978.4(ST14):c.2463C>T (p.Ala821=) rs141093713 0.00006
NM_021978.4(ST14):c.1408C>T (p.Arg470Cys) rs199767874 0.00005
NM_021978.4(ST14):c.2277C>A (p.Gly759=) rs748084680 0.00005
NM_021978.4(ST14):c.598+9G>A rs373568662 0.00003
NM_021978.4(ST14):c.1554C>T (p.Ser518=) rs533140977 0.00002
NM_021978.4(ST14):c.804C>T (p.Cys268=) rs370962804 0.00002
NM_021978.4(ST14):c.1223+15G>C rs779524328 0.00001
NM_021978.4(ST14):c.1015+9G>C rs1465753171
NM_021978.4(ST14):c.1170C>T (p.Pro390=)
NM_021978.4(ST14):c.1224-6dup rs11368852
NM_021978.4(ST14):c.1224-8_1224-7insT rs779187925
NM_021978.4(ST14):c.1230C>T (p.Cys410=)
NM_021978.4(ST14):c.1467C>T (p.Asp489=)
NM_021978.4(ST14):c.1557C>T (p.Asp519=) rs367833176
NM_021978.4(ST14):c.1571-4C>G
NM_021978.4(ST14):c.1727A>G (p.Asn576Ser)
NM_021978.4(ST14):c.1764C>T (p.Asp588=)
NM_021978.4(ST14):c.1770G>C (p.Lys590Asn)
NM_021978.4(ST14):c.1923C>T (p.Cys641=)
NM_021978.4(ST14):c.1975A>G (p.Ile659Val)
NM_021978.4(ST14):c.1994+20G>A
NM_021978.4(ST14):c.2004C>T (p.Asp668=) rs372683317
NM_021978.4(ST14):c.2187C>A (p.Pro729=)
NM_021978.4(ST14):c.21C>T (p.Arg7=)
NM_021978.4(ST14):c.2269+3A>G rs562346233
NM_021978.4(ST14):c.2415C>T (p.Ser805=)
NM_021978.4(ST14):c.330C>T (p.Ser110=)
NM_021978.4(ST14):c.36C>T (p.Gly12=)
NM_021978.4(ST14):c.492C>T (p.His164=)
NM_021978.4(ST14):c.513C>T (p.Arg171=)
NM_021978.4(ST14):c.585A>C (p.Ser195=) rs1591887587
NM_021978.4(ST14):c.635-5C>T rs199819888
NM_021978.4(ST14):c.639C>T (p.Ser213=)
NM_021978.4(ST14):c.753C>T (p.Asp251=)

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