ClinVar Miner

List of variants in gene ENG reported as uncertain significance for not provided

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Total variants: 13
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HGVS dbSNP
NM_000118.2(ENG):c.706_708delGTG (p.Val236del) rs1064794221
NM_000118.3(ENG):c.-79C>T
NM_000118.3(ENG):c.1089T>G (p.Cys363Trp)
NM_000118.3(ENG):c.137C>T (p.Thr46Ile) rs1393437924
NM_000118.3(ENG):c.158G>A (p.Cys53Tyr) rs187643086
NM_000118.3(ENG):c.512G>C (p.Arg171Pro) rs756980265
NM_000118.3(ENG):c.67+5G>A rs763111216
NM_000118.3(ENG):c.742_743insT (p.Asp248Valfs)
NM_000118.3(ENG):c.7C>T (p.Arg3Cys) rs139334561
NM_000118.3(ENG):c.98A>C (p.Gln33Pro) rs863223531
NM_001114753.2(ENG):c.1970T>C (p.Met657Thr) rs768873662
NM_001114753.2(ENG):c.687C>T (p.Ala229=) rs376919650
NM_001114753.2(ENG):c.788T>A (p.Ile263Asn) rs1085307431

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