PACRGL[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3207886	NM_001258345.3(PACRGL):c.11C>T (p.Ser4Leu)	PACRGL (S4L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303885	NM_001258345.3(PACRGL):c.38A>C (p.Lys13Thr)	PACRGL (K13T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264186	NM_001258345.3(PACRGL):c.70A>C (p.Thr24Pro)	PACRGL (T24P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522184	NM_001258345.3(PACRGL):c.106G>A (p.Val36Ile)	PACRGL (V36I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623855	NM_001258345.3(PACRGL):c.109C>A (p.Gln37Lys)	PACRGL (Q37K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491340	NM_001258345.3(PACRGL):c.116G>A (p.Ser39Asn)	PACRGL (S39N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3207887	NM_001258345.3(PACRGL):c.133A>G (p.Thr45Ala)	PACRGL (T45A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3207888	NM_001258345.3(PACRGL):c.360A>C (p.Leu120Phe)	PACRGL (L120F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3207889	NM_001258345.3(PACRGL):c.421G>A (p.Glu141Lys)	PACRGL (E88K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2556880	NM_001258345.3(PACRGL):c.506A>T (p.His169Leu)	PACRGL (H116L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240892	NM_001258345.3(PACRGL):c.596A>G (p.His199Arg)	PACRGL (H101R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244159	NM_001258345.3(PACRGL):c.604A>C (p.Thr202Pro)	PACRGL (T149P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269121	NM_001258345.3(PACRGL):c.721C>A (p.Pro241Thr)	PACRGL (P116T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance