Related gene-specific medical variations for Gene (Select 4762) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3299387	NM_006161.3(NEUROG1):c.149G>A (p.Arg50Lys)	LOC123497974, NEUROG1 (R50K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195493	NM_006161.3(NEUROG1):c.49A>G (p.Ser17Gly)	LOC123497974, NEUROG1 (S17G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195478	NM_006161.3(NEUROG1):c.44C>T (p.Ala15Val)	LOC123497974, NEUROG1 (A15V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195474	NM_006161.3(NEUROG1):c.43G>T (p.Ala15Ser)	LOC123497974, NEUROG1 (A15S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547316	NM_006161.3(NEUROG1):c.131C>T (p.Pro44Leu)	LOC123497974, NEUROG1 (P44L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385169	NM_006161.3(NEUROG1):c.115G>A (p.Ala39Thr)	LOC123497974, NEUROG1 (A39T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 738611	NM_006161.3(NEUROG1):c.141G>A (p.Pro47=)	LOC123497974, NEUROG1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 712449	NM_006161.3(NEUROG1):c.101G>A (p.Arg34Lys)	LOC123497974, NEUROG1 (R34K)	Single nucleotide variant (missense variant)	not provided	GBenign

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