PVRIG[gene] and "single gene"[properties] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3149896	NM_001397246.1(PVRIG):c.5G>C (p.Gly2Ala)	PVRIG (G22A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311755	NM_001397246.1(PVRIG):c.10C>T (p.Arg4Trp)	PVRIG (R4W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372015	NM_001397246.1(PVRIG):c.11G>A (p.Arg4Gln)	PVRIG (R24Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3149893	NM_001397246.1(PVRIG):c.44T>C (p.Leu15Ser)	PVRIG (L15S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254198	NM_001397246.1(PVRIG):c.94G>A (p.Ala32Thr)	PVRIG (A32T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343432	NM_001397246.1(PVRIG):c.107C>T (p.Ser36Leu)	PVRIG (S36L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520611	NM_001397246.1(PVRIG):c.122G>A (p.Arg41His)	PVRIG (R61H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3149894	NM_001397246.1(PVRIG):c.182A>G (p.Asn61Ser)	PVRIG (N81S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455283	NM_001397246.1(PVRIG):c.233G>A (p.Arg78Gln)	PVRIG (R78Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2296728	NM_001397246.1(PVRIG):c.245C>G (p.Pro82Arg)	PVRIG (P82R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271461	NM_001397246.1(PVRIG):c.326A>C (p.Asn109Thr)	PVRIG (N129T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465120	NM_001397246.1(PVRIG):c.392C>T (p.Pro131Leu)	PVRIG (P151L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2345330	NM_001397246.1(PVRIG):c.419C>T (p.Ala140Val)	PVRIG (A160V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393062	NM_001397246.1(PVRIG):c.422C>T (p.Pro141Leu)	PVRIG (P141L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373977	NM_001397246.1(PVRIG):c.445C>T (p.Arg149Trp)	PVRIG (R149W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277741	NM_001397246.1(PVRIG):c.499G>T (p.Val167Phe)	PVRIG (V187F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407009	NM_001397246.1(PVRIG):c.521G>A (p.Arg174His)	PVRIG (R194H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511821	NM_001397246.1(PVRIG):c.524G>A (p.Arg175Gln)	PVRIG (R175Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3149895	NM_001397246.1(PVRIG):c.539C>T (p.Pro180Leu)	PVRIG (P157L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311756	NM_001397246.1(PVRIG):c.562C>T (p.Arg188Cys)	PVRIG (R165C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482642	NM_001397246.1(PVRIG):c.570C>G (p.Ser190Arg)	PVRIG (S167R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311757	NM_001397246.1(PVRIG):c.581C>T (p.Pro194Leu)	PVRIG (P214L +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2601044	NM_001397246.1(PVRIG):c.656G>A (p.Ser219Asn)	PVRIG (S219N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396962	NM_001397246.1(PVRIG):c.661C>T (p.Arg221Cys)	PVRIG (R221C +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2399621	NM_001397246.1(PVRIG):c.739C>T (p.Arg247Trp)	PVRIG (R247W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3149897	NM_001397246.1(PVRIG):c.748G>A (p.Gly250Ser)	PVRIG (G270S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3311754	NM_001397246.1(PVRIG):c.764C>T (p.Ala255Val)	PVRIG (A232V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363110	NM_001397246.1(PVRIG):c.890G>A (p.Arg297Lys)	PVRIG (R274K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 28