Related gene-specific medical variations for Gene (Select 1212) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2531692	NM_007097.5(CLTB):c.61G>C (p.Glu21Gln)	CLTB, LOC129995335 (E21Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472541	NM_007097.5(CLTB):c.311G>A (p.Arg104His)	ARL10, CLTB (R104H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389379	NM_007097.5(CLTB):c.44C>T (p.Ala15Val)	CLTB, LOC129995335 (A15V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2285222	NM_007097.5(CLTB):c.94G>C (p.Glu32Gln)	CLTB, LOC129995335 (E32Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2283049	NM_007097.5(CLTB):c.47C>T (p.Pro16Leu)	CLTB, LOC129995335 (P16L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278818	NM_007097.5(CLTB):c.586G>A (p.Ala196Thr)	ARL10, CLTB (A111T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273130	NM_007097.5(CLTB):c.259T>C (p.Tyr87His)	ARL10, CLTB (Y87H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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