"Ambry Genetics"[submitter] AND "PRR16"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3219366	NM_001300783.2(PRR16):c.159+16610C>A	PRR16 (L18I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512464	NM_001300783.2(PRR16):c.207T>G (p.Asp69Glu)	PRR16 (D46E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205710	NM_001300783.2(PRR16):c.236C>T (p.Thr79Met)	PRR16 (T9M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539835	NM_001300783.2(PRR16):c.255T>A (p.Ser85Arg)	PRR16 (S15R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219364	NM_001300783.2(PRR16):c.262A>G (p.Thr88Ala)	PRR16 (T18A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223117	NM_001300783.2(PRR16):c.284T>C (p.Ile95Thr)	PRR16 (I25T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402847	NM_001300783.2(PRR16):c.344C>T (p.Thr115Met)	PRR16 (T115M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217492	NM_001300783.2(PRR16):c.374C>A (p.Pro125His)	PRR16 (P102H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219365	NM_001300783.2(PRR16):c.439G>T (p.Val147Leu)	PRR16 (V77L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310446	NM_001300783.2(PRR16):c.460C>G (p.Leu154Val)	PRR16 (L154V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594297	NM_001300783.2(PRR16):c.509A>G (p.Asp170Gly)	PRR16 (D100G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378690	NM_001300783.2(PRR16):c.611G>A (p.Arg204Gln)	PRR16 (R134Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219367	NM_001300783.2(PRR16):c.635A>G (p.Gln212Arg)	PRR16 (Q189R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218216	NM_001300783.2(PRR16):c.668G>C (p.Arg223Pro)	PRR16 (R153P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370211	NM_001300783.2(PRR16):c.797G>C (p.Gly266Ala)	PRR16 (G266A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458940	NM_001300783.2(PRR16):c.829C>A (p.Pro277Thr)	PRR16 (P254T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266982	NM_001300783.2(PRR16):c.877A>C (p.Lys293Gln)	PRR16 (K223Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance