ClinVar Miner

List of variants reported as benign for Usher syndrome, type 1C

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Total variants: 17
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HGVS dbSNP
NM_005709.4(USH1C):c.*218C>T rs1055577
NM_005709.4(USH1C):c.*243A>G rs1055581
NM_005709.4(USH1C):c.*78T>C rs1055574
NM_005709.4(USH1C):c.-60T>C rs371444878
NM_005709.4(USH1C):c.1086-12G>A rs11024318
NM_005709.4(USH1C):c.1188A>G (p.Pro396=) rs2240487
NM_005709.4(USH1C):c.1243G>A (p.Ala415Thr) rs116996553
NM_005709.4(USH1C):c.1261G>A (p.Gly421Ser) rs115931035
NM_005709.4(USH1C):c.1326+12C>T rs17703528
NM_005709.4(USH1C):c.1440C>T (p.Val480=) rs10832796
NM_005709.4(USH1C):c.1557G>C (p.Glu519Asp) rs1064074
NM_005709.4(USH1C):c.1590+12G>C rs2072232
NM_005709.4(USH1C):c.225T>C (p.Asp75=) rs111033279
NM_005709.4(USH1C):c.651A>G (p.Val217=) rs75977878
NM_153676.4(USH1C):c.294C>T (p.Leu98=) rs34055234
NM_153676.4(USH1C):c.388G>A (p.Val130Ile) rs55843567
NM_153676.4(USH1C):c.496+21GCAGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGG[9] rs55983148

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