List of variants in gene GLYCTK reported as uncertain significance for carbohydrate metabolism disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_145262.4(GLYCTK):c.791T>A (p.Val264Glu)	rs73088796	0.00091
NM_145262.4(GLYCTK):c.384G>C (p.Met128Ile)	rs150662353	0.00090
NM_145262.4(GLYCTK):c.1460A>G (p.Asn487Ser)	rs767047161	0.00019
NM_145262.4(GLYCTK):c.1313C>T (p.Pro438Leu)	rs758823918	0.00009
NM_145262.4(GLYCTK):c.1478T>G (p.Phe493Cys)	rs121909448	0.00009
NM_145262.4(GLYCTK):c.457C>T (p.Arg153Trp)	rs199906865	0.00009
NM_145262.4(GLYCTK):c.1036C>G (p.Gln346Glu)	rs773672318	0.00003
NM_145262.4(GLYCTK):c.425C>T (p.Ala142Val)	rs762737029	0.00003
NM_145262.4(GLYCTK):c.37C>T (p.Arg13Ter)	rs910401729	0.00002
NM_145262.4(GLYCTK):c.112G>A (p.Ala38Thr)	rs1700426072
NM_145262.4(GLYCTK):c.1132G>A (p.Ala378Thr)	rs1186216170
NM_145262.4(GLYCTK):c.304G>A (p.Gly102Ser)	rs558300707
NM_145262.4(GLYCTK):c.550C>T (p.Pro184Ser)	rs1379123977
NM_145262.4(GLYCTK):c.60_62del (p.Trp21del)	rs1553621315
NM_145262.4(GLYCTK):c.967G>A (p.Ala323Thr)	rs753867724

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