Related gene-specific medical variations for Gene (Select 440574) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3126299	NM_001032363.4(MICOS10):c.68C>G (p.Thr23Ser)	MICOS10, MICOS10-NBL1 (T23S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3126298	NM_001032363.4(MICOS10):c.62T>C (p.Ile21Thr)	MICOS10, MICOS10-NBL1 (I21T)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3126297	NM_001032363.4(MICOS10):c.47A>G (p.Asp16Gly)	MICOS10, MICOS10-NBL1 (D16G)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3126296	NM_001032363.4(MICOS10):c.44C>T (p.Ala15Val)	MICOS10, MICOS10-NBL1 (A15V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3126295	NM_001032363.4(MICOS10):c.223-836C>A	MICOS10, MICOS10-NBL1 (P128T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126294	NM_001032363.4(MICOS10):c.14A>C (p.Glu5Ala)	LOC129929576, MICOS10 +1 more (E5A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2611948	NM_001032363.4(MICOS10):c.220A>C (p.Lys74Gln)	MICOS10, MICOS10-NBL1 (K58Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2603808	NM_001032363.4(MICOS10):c.7G>A (p.Glu3Lys)	LOC129929576, MICOS10 +1 more (E3K)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance