ClinVar Miner

List of variants in gene SETX reported as likely benign for not specified

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_015046.7(SETX):c.1077T>C (p.Tyr359=) rs9411449
NM_015046.7(SETX):c.1221A>G (p.Thr407=)
NM_015046.7(SETX):c.3090T>C (p.Leu1030=) rs368677513
NM_015046.7(SETX):c.3336T>C (p.Ala1112=) rs150687078
NM_015046.7(SETX):c.3345C>G (p.Ala1115=) rs142020270
NM_015046.7(SETX):c.3455T>G (p.Phe1152Cys) rs3739922
NM_015046.7(SETX):c.3576T>G (p.Asp1192Glu) rs1185193
NM_015046.7(SETX):c.3754G>A (p.Gly1252Arg) rs1183768
NM_015046.7(SETX):c.390C>T (p.Asn130=)
NM_015046.7(SETX):c.4156A>G (p.Ile1386Val) rs543573
NM_015046.7(SETX):c.4660T>G (p.Cys1554Gly) rs112089123
NM_015046.7(SETX):c.5563A>G (p.Thr1855Ala) rs2296871
NM_015046.7(SETX):c.5811T>C (p.Asp1937=) rs2296869
NM_015046.7(SETX):c.5825T>C (p.Ile1942Thr)
NM_015046.7(SETX):c.5950-14G>A rs375632375
NM_015046.7(SETX):c.719-40T>G rs756527948
NM_015046.7(SETX):c.7640T>C (p.Ile2547Thr) rs151117904
NM_015046.7(SETX):c.7749C>T (p.Asp2583=) rs754701648
NM_015046.7(SETX):c.7759A>G (p.Ile2587Val) rs1056899

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