ClinVar Miner

List of variants in gene SZT2 reported as likely benign for not specified

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Total variants: 25
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HGVS dbSNP
NM_015284.3(SZT2):c.1107A>G (p.Leu369=) rs533632273
NM_015284.3(SZT2):c.1770-11C>T rs756655876
NM_015284.3(SZT2):c.1791C>T (p.His597=) rs151110718
NM_015284.3(SZT2):c.2025G>A (p.Pro675=) rs561698107
NM_015284.3(SZT2):c.2356C>T (p.Leu786=) rs878855007
NM_015284.3(SZT2):c.2547T>A (p.Ile849=) rs774483969
NM_015284.3(SZT2):c.2550+5G>A rs41270349
NM_015284.3(SZT2):c.2631C>T (p.Thr877=) rs140831372
NM_015284.3(SZT2):c.2930-4G>A rs780736141
NM_015284.3(SZT2):c.3045T>C (p.Gly1015=) rs763882399
NM_015284.3(SZT2):c.3138+9C>T rs140366288
NM_015284.3(SZT2):c.3633-9G>A rs138670520
NM_015284.3(SZT2):c.3753A>G (p.Leu1251=) rs1060504947
NM_015284.3(SZT2):c.4005C>T (p.Thr1335=) rs373047934
NM_015284.3(SZT2):c.4310-5A>G rs878855008
NM_015284.3(SZT2):c.588G>A (p.Lys196=) rs774244334
NM_015284.3(SZT2):c.5946C>T (p.Asp1982=) rs756197807
NM_015284.3(SZT2):c.6209A>T (p.Tyr2070Phe) rs149812437
NM_015284.3(SZT2):c.6372A>G (p.Leu2124=) rs112461557
NM_015284.3(SZT2):c.7104T>C (p.Pro2368=) rs771745066
NM_015284.3(SZT2):c.7224T>C (p.Ile2408=) rs78858677
NM_015284.3(SZT2):c.7272C>T (p.Thr2424=) rs760714768
NM_015284.3(SZT2):c.7860G>A (p.Ala2620=) rs138303356
NM_015284.3(SZT2):c.8827-6delC rs536641188
NM_015284.3(SZT2):c.9189T>C (p.Ser3063=) rs367855839

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