ClinVar Miner

List of variants in gene GALT reported as likely benign

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Total variants: 36
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HGVS dbSNP
NM_000155.4(GALT):c.1059+24G>A rs111033840
NM_000155.4(GALT):c.1071A>G (p.Arg357=)
NM_000155.4(GALT):c.1077G>A (p.Arg359=)
NM_000155.4(GALT):c.1116C>T (p.Asp372=)
NM_000155.4(GALT):c.1128A>T (p.Ala376=) rs781374930
NM_000155.4(GALT):c.1135G>A (p.Ala379Thr)
NM_000155.4(GALT):c.231G>A (p.Gly77=)
NM_000155.4(GALT):c.267C>T (p.Tyr89=)
NM_000155.4(GALT):c.291C>T (p.Asn97=) rs398123180
NM_000155.4(GALT):c.328+7T>C rs774350978
NM_000155.4(GALT):c.329-24G>A rs114539202
NM_000155.4(GALT):c.378-9A>G
NM_000155.4(GALT):c.390C>T (p.Cys130=) rs1410761611
NM_000155.4(GALT):c.414G>A (p.Thr138=)
NM_000155.4(GALT):c.414G>T (p.Thr138=) rs116479817
NM_000155.4(GALT):c.450T>A (p.Val150=) rs886063884
NM_000155.4(GALT):c.459A>G (p.Ala153=)
NM_000155.4(GALT):c.480G>A (p.Glu160=)
NM_000155.4(GALT):c.498T>C (p.Pro166=) rs193922249
NM_000155.4(GALT):c.564+15G>A rs111033732
NM_000155.4(GALT):c.564+7G>A rs760189807
NM_000155.4(GALT):c.652C>T (p.Leu218=) rs2070075
NM_000155.4(GALT):c.678A>G (p.Leu226=) rs777577533
NM_000155.4(GALT):c.687+9G>C rs117998880
NM_000155.4(GALT):c.688-4C>T rs374014228
NM_000155.4(GALT):c.700C>T (p.Leu234=)
NM_000155.4(GALT):c.753C>T (p.Tyr251=) rs367543261
NM_000155.4(GALT):c.799C>T (p.Leu267=) rs764006034
NM_000155.4(GALT):c.82+8C>T
NM_000155.4(GALT):c.821-46G>T rs111033776
NM_000155.4(GALT):c.83-46G>C rs201156392
NM_000155.4(GALT):c.876G>A (p.Thr292=) rs1055607
NM_000155.4(GALT):c.885C>G (p.Pro295=) rs1554709446
NM_000155.4(GALT):c.919T>A (p.Ser307Thr)
NM_000155.4(GALT):c.940A>G (p.Asn314Asp) rs2070074
NM_000155.4(GALT):c.945T>C (p.His315=) rs61735982

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