List of variants in gene GALT reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000155.4(GALT):c.940A>G (p.Asn314Asp)	rs2070074	0.07150
NM_000155.4(GALT):c.510C>A (p.Ile170=)	rs61735984	0.00290
NM_000155.4(GALT):c.563A>G (p.Gln188Arg)	rs75391579	0.00192
NM_000155.4(GALT):c.498T>C (p.Pro166=)	rs193922249	0.00029
NM_000155.4(GALT):c.855G>T (p.Lys285Asn)	rs111033773	0.00017
NM_000155.4(GALT):c.584T>C (p.Leu195Pro)	rs111033728	0.00006
NM_000155.4(GALT):c.425T>A (p.Met142Lys)	rs111033695	0.00001
NM_000155.4(GALT):c.593T>C (p.Ile198Thr)	rs1483461355	0.00001
NM_000155.4(GALT):c.663C>T (p.Tyr221=)	rs755000603	0.00001
NM_000155.4(GALT):c.974C>T (p.Pro325Leu)	rs111033794	0.00001
NM_000155.4(GALT):c.-119_-116delGTCA	rs111033640
NM_000155.4(GALT):c.414G>T (p.Thr138=)	rs116479817
NM_000155.4(GALT):c.460T>C (p.Trp154Arg)	rs111033702
NM_000155.4(GALT):c.957C>A (p.His319Gln)	rs111033792

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