ClinVar Miner

List of variants in gene OBSL1 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_015311.3(OBSL1):c.3752C>T (p.Pro1251Leu) rs145485683 0.01074
NM_015311.3(OBSL1):c.5202C>A (p.Asp1734Glu) rs181520135 0.00757
NM_015311.3(OBSL1):c.4361G>A (p.Arg1454Gln) rs183329050 0.00737
NM_015311.3(OBSL1):c.3003C>T (p.Ala1001=) rs150691758 0.00634
NM_015311.3(OBSL1):c.4732C>T (p.Gln1578Ter) rs116131367 0.00337
NM_015311.3(OBSL1):c.3816C>T (p.Pro1272=) rs200349173 0.00270
NM_015311.3(OBSL1):c.1734G>A (p.Pro578=) rs181182663 0.00256
NM_015311.3(OBSL1):c.2238G>A (p.Pro746=) rs142650279 0.00255
NM_015311.3(OBSL1):c.1255C>T (p.Arg419Cys) rs79295927 0.00155
NM_015311.3(OBSL1):c.762C>T (p.Thr254=) rs199929590 0.00138
NM_015311.3(OBSL1):c.4069C>T (p.Pro1357Ser) rs200543358 0.00098
NM_015311.3(OBSL1):c.79G>A (p.Ala27Thr) rs373427330 0.00039
NM_015311.3(OBSL1):c.4588C>T (p.Leu1530=) rs201893489 0.00026
NM_015311.3(OBSL1):c.2595G>A (p.Val865=) rs368895697 0.00014
NM_015311.3(OBSL1):c.3850G>A (p.Gly1284Ser) rs74589174 0.00014
NM_015311.3(OBSL1):c.342C>T (p.Ala114=) rs760053992 0.00009
NM_015311.3(OBSL1):c.4133C>T (p.Thr1378Met) rs200449388 0.00009
NM_015311.3(OBSL1):c.2175G>A (p.Ser725=) rs376487302 0.00008
NM_015311.3(OBSL1):c.3292C>T (p.Arg1098Cys) rs768636811 0.00004
NM_015311.3(OBSL1):c.1474G>A (p.Ala492Thr) rs747339260 0.00001
NM_015311.3(OBSL1):c.2886C>T (p.Leu962=) rs757808976 0.00001
NM_015311.3(OBSL1):c.3067T>C (p.Tyr1023His) rs753558905 0.00001
NM_015311.3(OBSL1):c.3236A>T (p.Glu1079Val) rs775467805 0.00001
NM_015311.3(OBSL1):c.3853G>A (p.Gly1285Arg) rs570704076 0.00001
NM_015311.3(OBSL1):c.4396G>A (p.Val1466Met) rs1408776700 0.00001
NM_015311.3(OBSL1):c.4453C>T (p.Arg1485Ter) rs568750433 0.00001
NM_015311.3(OBSL1):c.1424G>A (p.Ser475Asn) rs1214483288
NM_015311.3(OBSL1):c.180C>T (p.Phe60=)
NM_015311.3(OBSL1):c.188A>G (p.Asp63Gly) rs1364672065
NM_015311.3(OBSL1):c.2895C>T (p.Ser965=)
NM_015311.3(OBSL1):c.3402del (p.Thr1135fs) rs1449351602
NM_015311.3(OBSL1):c.3475G>T (p.Ala1159Ser)
NM_015311.3(OBSL1):c.3596G>A (p.Arg1199Gln)
NM_015311.3(OBSL1):c.3731C>T (p.Thr1244Ile)
NM_015311.3(OBSL1):c.3974T>C (p.Val1325Ala)
NM_015311.3(OBSL1):c.4005C>A (p.Asp1335Glu) rs375716830
NM_015311.3(OBSL1):c.4005C>T (p.Asp1335=) rs375716830
NM_015311.3(OBSL1):c.4951G>T (p.Glu1651Ter) rs140825693
NM_015311.3(OBSL1):c.5210C>A (p.Thr1737Lys) rs199594182
NM_015311.3(OBSL1):c.537C>T (p.Leu179=)
NM_015311.3(OBSL1):c.892C>T (p.Arg298Cys)

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