Related gene-specific medical variations for Gene (Select 4681) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3126311	NM_001204088.2(MICOS10-NBL1):c.529C>T (p.Pro177Ser)	MICOS10-NBL1, NBL1 (P177S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126310	NM_001204088.2(MICOS10-NBL1):c.520G>A (p.Gly174Arg)	MICOS10-NBL1, NBL1 (G174R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126309	NM_001204088.2(MICOS10-NBL1):c.481G>A (p.Gly161Ser)	MICOS10-NBL1, NBL1 (G147S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126308	NM_001204088.2(MICOS10-NBL1):c.449T>C (p.Val150Ala)	MICOS10-NBL1, NBL1 (V150A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126307	NM_001204088.2(MICOS10-NBL1):c.442G>C (p.Val148Leu)	MICOS10-NBL1, NBL1 (V169L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126306	NM_001204088.2(MICOS10-NBL1):c.432G>C (p.Glu144Asp)	MICOS10-NBL1, NBL1 (E164D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126305	NM_001204088.2(MICOS10-NBL1):c.407C>A (p.Ala136Asp)	MICOS10-NBL1, NBL1 (A136D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126304	NM_001204088.2(MICOS10-NBL1):c.406G>A (p.Ala136Thr)	MICOS10-NBL1, NBL1 (A122T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126303	NM_001204088.2(MICOS10-NBL1):c.359C>A (p.Pro120His)	MICOS10-NBL1, NBL1 (P106H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126302	NM_001204088.2(MICOS10-NBL1):c.341C>T (p.Pro114Leu)	MICOS10-NBL1, NBL1 (P100L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126301	NM_001204088.2(MICOS10-NBL1):c.227A>G (p.Gln76Arg)	MICOS10-NBL1, NBL1 (Q62R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359745	NM_182744.4(NBL1):c.55C>T (p.Pro19Ser)	MICOS10-NBL1, NBL1 (P19S)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance