Related gene-specific medical variations for Gene (Select 11132) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3263151	NM_023083.4(CAPN10):c.42C>G (p.Phe14Leu)	CAPN10, LOC112840920 (F14L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3263149	NM_023083.4(CAPN10):c.8C>T (p.Ala3Val)	CAPN10, LOC112840920 (A3V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3137024	NM_023083.4(CAPN10):c.136C>T (p.Pro46Ser)	CAPN10, LOC112840920 (P46S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2335548	NM_023083.4(CAPN10):c.25C>T (p.Pro9Ser)	CAPN10, LOC112840920 (P9S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2297433	NM_023083.4(CAPN10):c.125C>T (p.Thr42Met)	CAPN10, LOC112840920 (T42M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 716765	NM_023083.4(CAPN10):c.100C>G (p.Leu34Val)	CAPN10, LOC112840920 (L34V)	Single nucleotide variant (missense variant)	not provided	GBenign

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