ClinVar Miner

List of variants in gene STRC reported as uncertain significance for not specified

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Gene type:
ClinVar version:
Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_153700.2(STRC):c.3218G>A (p.Arg1073Gln) rs727503449 0.00085
NM_153700.2(STRC):c.4432A>C (p.Thr1478Pro) rs148736697 0.00051
NM_153700.2(STRC):c.890A>G (p.Asn297Ser) rs876658011 0.00038
NM_153700.2(STRC):c.2640G>T (p.Glu880Asp) rs1342864499 0.00017
NM_153700.2(STRC):c.4466A>C (p.Glu1489Ala) rs200009157 0.00017
NM_153700.2(STRC):c.3307-5T>G rs727503446 0.00014
NM_153700.2(STRC):c.3817T>C (p.Ser1273Pro) rs144626173 0.00011
NM_153700.2(STRC):c.2494C>T (p.Arg832Trp) rs876658007 0.00005
NM_153700.2(STRC):c.2495G>A (p.Arg832Gln) rs1425015832 0.00005
NM_153700.2(STRC):c.3275G>A (p.Cys1092Tyr) rs727503447 0.00005
NM_153700.2(STRC):c.3307G>A (p.Val1103Ile) rs1057518394 0.00004
NM_153700.2(STRC):c.3794C>T (p.Pro1265Leu) rs371994634 0.00004
NM_153700.2(STRC):c.2527A>G (p.Lys843Glu) rs1321776840 0.00003
NM_153700.2(STRC):c.2481-3C>A rs1378890067 0.00002
NM_153700.2(STRC):c.3661A>C (p.Thr1221Pro) rs780948412 0.00002
NM_153700.2(STRC):c.3404T>G (p.Leu1135Arg) rs876658009 0.00001
NM_153700.2(STRC):c.4279A>G (p.Ser1427Gly) rs760961629 0.00001
NM_153700.2(STRC):c.436G>A (p.Gly146Arg) rs757152351 0.00001
NM_153700.2(STRC):c.4792C>G (p.Leu1598Val) rs753942597 0.00001
NC_000015.9:g.(?_43891870)_(43897597_?)dup
NC_000015.9:g.(?_43892732)_(43893212_?)dup
NC_000015.9:g.(?_43892732)_(43901532_?)dup
NC_000015.9:g.(?_43893070)_(43903182_?)dup
NC_000015.9:g.(?_43900061)_(43901532_?)dup
NM_153700.2(STRC):c.(?_3499)-60_(3557_?)+31del
NM_153700.2(STRC):c.(?_3519)_(3557_?)+28dup
NM_153700.2(STRC):c.(?_4443)_(4845_?)-68dup
NM_153700.2(STRC):c.(?_4845)-59_(4993_?)+61dup
NM_153700.2(STRC):c.1613G>T (p.Cys538Phe) rs876658006
NM_153700.2(STRC):c.2303_2313+1del rs1021413948
NM_153700.2(STRC):c.2614C>T (p.Pro872Ser) rs1187842173
NM_153700.2(STRC):c.2914C>T (p.Arg972Trp) rs876658008
NM_153700.2(STRC):c.3401T>G (p.Leu1134Arg) rs1555447461
NM_153700.2(STRC):c.4171C>T (p.Arg1391Cys) rs376104748
NM_153700.2(STRC):c.4298G>A (p.Cys1433Tyr) rs202189597
NM_153700.2(STRC):c.4415C>A (p.Pro1472Gln) rs144622511
NM_153700.2(STRC):c.4559C>A (p.Pro1520His) rs1246240978
NM_153700.2(STRC):c.4917_4918delinsCT (p.Leu1640Phe) rs727503441
NM_153700.2(STRC):c.4919T>G (p.Leu1640Arg) rs727503440
NM_153700.2(STRC):c.5129_5130delinsAG (p.Ser1710Lys) rs1555446762
NM_153700.2(STRC):c.877G>A (p.Gly293Ser) rs876658010
NM_153700.2(STRC):c.911C>T (p.Ala304Val) rs727503448
NM_153700.2(STRC):c.995C>G (p.Ser332Cys) rs1360568237

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