ClinVar Miner

List of variants in gene C9 reported as 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_001737.5(C9):c.78-10G>A rs476569 0.60021
NM_001737.5(C9):c.13C>T (p.Arg5Trp) rs700233 0.35371
NM_001737.5(C9):c.77+16T>C rs6864541 0.08814
NM_001737.5(C9):c.607A>G (p.Ile203Val) rs13361416 0.03247
NM_001737.5(C9):c.1645+14A>G rs700180 0.01978
NM_001737.5(C9):c.1065C>G (p.Leu355=) rs35460483 0.01447
NM_001737.5(C9):c.1279T>A (p.Ser427Thr) rs34421659 0.01154
NM_001737.5(C9):c.379G>T (p.Asp127Tyr) rs696763 0.01089
NM_001737.5(C9):c.636C>T (p.Phe212=) rs114751055 0.00927
NM_001737.5(C9):c.534T>C (p.Asn178=) rs76184752 0.00918
NM_001737.5(C9):c.836C>G (p.Thr279Ser) rs34625111 0.00560
NM_001737.5(C9):c.387A>C (p.Ser129=) rs147450097 0.00427
NM_001737.5(C9):c.1646-3T>C rs141471456 0.00361
NM_001737.5(C9):c.652G>A (p.Glu218Lys) rs148389506 0.00163
NM_001737.5(C9):c.929A>G (p.Asn310Ser) rs200511324 0.00086
NM_001737.5(C9):c.835A>G (p.Thr279Ala) rs183125896 0.00082
NM_001737.5(C9):c.615+12C>T rs376805303 0.00044
NM_001737.5(C9):c.417T>C (p.Arg139=) rs201897029 0.00007
NM_001737.5(C9):c.1401T>G (p.Val467=) rs201909611 0.00006
NM_001737.5(C9):c.476+11dup rs2111952646
NM_001737.5(C9):c.624C>A (p.Gly208=) rs139000312
NM_001737.5(C9):c.72G>A (p.Thr24=)

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