ClinVar for Gene (Select 7916) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 259

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3355698	NM_004638.4(PRRC2A):c.5862G>A (p.Ser1954=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GLikely benign
Select item 3310539	NM_004638.4(PRRC2A):c.3791G>A (p.Arg1264Gln)	PRRC2A (R1264Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310538	NM_004638.4(PRRC2A):c.4348C>T (p.Leu1450Phe)	PRRC2A (L1450F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310537	NM_004638.4(PRRC2A):c.3925C>G (p.Leu1309Val)	PRRC2A (L1309V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310536	NM_004638.4(PRRC2A):c.5143C>A (p.His1715Asn)	PRRC2A (H1715N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310535	NM_004638.4(PRRC2A):c.2786G>A (p.Arg929His)	PRRC2A (R929H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310534	NM_004638.4(PRRC2A):c.2654C>T (p.Pro885Leu)	PRRC2A (P885L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310533	NM_004638.4(PRRC2A):c.1271G>C (p.Gly424Ala)	PRRC2A (G424A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310532	NM_004638.4(PRRC2A):c.3173G>T (p.Arg1058Leu)	PRRC2A (R1058L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310529	NM_004638.4(PRRC2A):c.1249C>T (p.Arg417Trp)	PRRC2A (R417W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310528	NM_004638.4(PRRC2A):c.2446G>A (p.Glu816Lys)	PRRC2A (E816K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310527	NM_004638.4(PRRC2A):c.1508G>A (p.Arg503Gln)	PRRC2A (R503Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310526	NM_004638.4(PRRC2A):c.5117C>G (p.Pro1706Arg)	PRRC2A (P1706R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310525	NM_004638.4(PRRC2A):c.3533C>T (p.Pro1178Leu)	PRRC2A (P1178L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310524	NM_004638.4(PRRC2A):c.3822G>T (p.Lys1274Asn)	PRRC2A (K1274N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310523	NM_004638.4(PRRC2A):c.866G>A (p.Arg289Gln)	PRRC2A (R289Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219623	NM_004638.4(PRRC2A):c.857C>T (p.Ala286Val)	PRRC2A (A286V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219622	NM_004638.4(PRRC2A):c.782T>G (p.Phe261Cys)	PRRC2A (F261C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219621	NM_004638.4(PRRC2A):c.637C>T (p.Arg213Cys)	PRRC2A (R213C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219620	NM_004638.4(PRRC2A):c.6374G>C (p.Trp2125Ser)	PRRC2A (W2125S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219618	NM_004638.4(PRRC2A):c.6224G>A (p.Arg2075Gln)	PRRC2A (R2075Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219617	NM_004638.4(PRRC2A):c.6004C>T (p.Pro2002Ser)	PRRC2A (P2002S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219616	NM_004638.4(PRRC2A):c.599G>A (p.Arg200His)	PRRC2A (R200H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219615	NM_004638.4(PRRC2A):c.5836G>A (p.Val1946Ile)	PRRC2A (V1946I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219614	NM_004638.4(PRRC2A):c.5354T>C (p.Leu1785Pro)	PRRC2A (L1785P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219613	NM_004638.4(PRRC2A):c.5230G>A (p.Gly1744Ser)	PRRC2A (G1744S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219611	NM_004638.4(PRRC2A):c.5143C>T (p.His1715Tyr)	PRRC2A (H1715Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219610	NM_004638.4(PRRC2A):c.5054A>C (p.Lys1685Thr)	PRRC2A (K1685T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219609	NM_004638.4(PRRC2A):c.4696A>G (p.Arg1566Gly)	PRRC2A (R1566G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219607	NM_004638.4(PRRC2A):c.4553A>T (p.Tyr1518Phe)	PRRC2A (Y1518F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219606	NM_004638.4(PRRC2A):c.4544C>T (p.Pro1515Leu)	PRRC2A (P1515L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219605	NM_004638.4(PRRC2A):c.4480G>A (p.Gly1494Arg)	PRRC2A (G1494R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219604	NM_004638.4(PRRC2A):c.433G>A (p.Ala145Thr)	PRRC2A (A145T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219603	NM_004638.4(PRRC2A):c.4337G>A (p.Arg1446His)	PRRC2A (R1446H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219602	NM_004638.4(PRRC2A):c.4192C>T (p.Arg1398Cys)	PRRC2A (R1398C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219601	NM_004638.4(PRRC2A):c.415G>A (p.Val139Ile)	PRRC2A (V139I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219600	NM_004638.4(PRRC2A):c.3884T>C (p.Val1295Ala)	PRRC2A (V1295A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219599	NM_004638.4(PRRC2A):c.3862G>A (p.Glu1288Lys)	PRRC2A (E1288K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219598	NM_004638.4(PRRC2A):c.3773G>A (p.Arg1258Gln)	PRRC2A (R1258Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219597	NM_004638.4(PRRC2A):c.3716G>A (p.Arg1239Gln)	PRRC2A (R1239Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219596	NM_004638.4(PRRC2A):c.3650C>G (p.Pro1217Arg)	PRRC2A (P1217R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219595	NM_004638.4(PRRC2A):c.3572C>T (p.Ser1191Phe)	PRRC2A (S1191F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219594	NM_004638.4(PRRC2A):c.3467G>A (p.Arg1156Gln)	PRRC2A (R1156Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219593	NM_004638.4(PRRC2A):c.3182G>A (p.Arg1061Gln)	PRRC2A (R1061Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219592	NM_004638.4(PRRC2A):c.3163C>T (p.Arg1055Cys)	PRRC2A (R1055C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219591	NM_004638.4(PRRC2A):c.314C>T (p.Pro105Leu)	PRRC2A (P105L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219590	NM_004638.4(PRRC2A):c.3090G>C (p.Glu1030Asp)	PRRC2A (E1030D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219589	NM_004638.4(PRRC2A):c.2998A>C (p.Asn1000His)	PRRC2A (N1000H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219588	NM_004638.4(PRRC2A):c.2954A>G (p.Lys985Arg)	PRRC2A (K985R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219587	NM_004638.4(PRRC2A):c.2843G>T (p.Arg948Leu)	PRRC2A (R948L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219586	NM_004638.4(PRRC2A):c.2804G>A (p.Arg935His)	PRRC2A (R935H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219584	NM_004638.4(PRRC2A):c.2719G>A (p.Gly907Arg)	PRRC2A (G907R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219583	NM_004638.4(PRRC2A):c.2624A>G (p.Lys875Arg)	PRRC2A (K875R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219582	NM_004638.4(PRRC2A):c.2576C>T (p.Pro859Leu)	PRRC2A (P859L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219581	NM_004638.4(PRRC2A):c.2558G>A (p.Arg853His)	PRRC2A (R853H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219580	NM_004638.4(PRRC2A):c.2246A>G (p.His749Arg)	PRRC2A (H749R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219579	NM_004638.4(PRRC2A):c.1985A>C (p.His662Pro)	PRRC2A (H662P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219578	NM_004638.4(PRRC2A):c.1693G>C (p.Ala565Pro)	PRRC2A (A565P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3219576	NM_004638.4(PRRC2A):c.1543C>T (p.Pro515Ser)	PRRC2A (P515S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219575	NM_004638.4(PRRC2A):c.1406G>A (p.Arg469Gln)	PRRC2A (R469Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219574	NM_004638.4(PRRC2A):c.1295G>A (p.Arg432His)	PRRC2A (R432H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219573	NM_004638.4(PRRC2A):c.1235T>A (p.Leu412Gln)	PRRC2A (L412Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219572	NM_004638.4(PRRC2A):c.1093T>G (p.Ser365Ala)	PRRC2A (S365A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3060526	NM_004638.4(PRRC2A):c.1062T>A (p.Gly354=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3060509	NM_004638.4(PRRC2A):c.5568A>G (p.Gln1856=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3060262	NM_004638.4(PRRC2A):c.5219G>A (p.Arg1740His)	PRRC2A (R1740H)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3060217	NM_004638.4(PRRC2A):c.6389C>T (p.Pro2130Leu)	PRRC2A (P2130L)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3060200	NM_004638.4(PRRC2A):c.1631C>A (p.Thr544Lys)	PRRC2A (T544K)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3060072	NM_004638.4(PRRC2A):c.4508T>C (p.Leu1503Pro)	PRRC2A (L1503P)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3059974	NM_004638.4(PRRC2A):c.317C>T (p.Pro106Leu)	PRRC2A (P106L)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3059883	NM_004638.4(PRRC2A):c.5649C>G (p.Pro1883=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3059796	NM_004638.4(PRRC2A):c.5683T>G (p.Leu1895Val)	PRRC2A (L1895V)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3059728	NM_004638.4(PRRC2A):c.2376A>G (p.Val792=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3058971	NM_004638.4(PRRC2A):c.6016C>T (p.Pro2006Ser)	PRRC2A (P2006S)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3057811	NM_004638.4(PRRC2A):c.222C>T (p.Pro74=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GLikely benign
Select item 3057656	NM_004638.4(PRRC2A):c.5031G>A (p.Lys1677=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GLikely benign
Select item 3057120	NM_004638.4(PRRC2A):c.5320G>A (p.Val1774Met)	PRRC2A (V1774M)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3056213	NM_004638.4(PRRC2A):c.5904C>A (p.Gly1968=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3056056	NM_004638.4(PRRC2A):c.2088A>C (p.Pro696=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3056032	NM_004638.4(PRRC2A):c.2094G>C (p.Pro698=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3056017	NM_004638.4(PRRC2A):c.636G>T (p.Gly212=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3055998	NM_004638.4(PRRC2A):c.1533_1544del (p.508PAAP[1])	PRRC2A	Deletion	PRRC2A-related disorder	GBenign
Select item 3055859	NM_004638.4(PRRC2A):c.4688G>A (p.Arg1563Gln)	PRRC2A (R1563Q)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3055740	NM_004638.4(PRRC2A):c.3144A>G (p.Gly1048=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3055620	NM_004638.4(PRRC2A):c.1544C>T (p.Pro515Leu)	PRRC2A (P515L)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3055548	NM_004638.4(PRRC2A):c.6248T>C (p.Phe2083Ser)	PRRC2A (F2083S)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3055429	NM_004638.4(PRRC2A):c.5297A>G (p.Asp1766Gly)	PRRC2A (D1766G)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3055264	NM_004638.4(PRRC2A):c.3656C>A (p.Ser1219Tyr)	PRRC2A (S1219Y)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3055241	NM_004638.4(PRRC2A):c.3106A>C (p.Arg1036=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GBenign
Select item 3054765	NM_004638.4(PRRC2A):c.923A>G (p.Lys308Arg)	PRRC2A (K308R)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GUncertain significance
Select item 3053226	NM_004638.4(PRRC2A):c.5856C>G (p.Ser1952=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GLikely benign
Select item 3053072	NM_004638.4(PRRC2A):c.858G>C (p.Ala286=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GLikely benign
Select item 3052626	NM_004638.4(PRRC2A):c.3847G>A (p.Ala1283Thr)	PRRC2A (A1283T)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3052538	NM_004638.4(PRRC2A):c.4220G>A (p.Ser1407Asn)	PRRC2A (S1407N)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3052409	NM_004638.4(PRRC2A):c.4344G>A (p.Pro1448=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GLikely benign
Select item 3052097	NM_004638.4(PRRC2A):c.4720-6C>G	PRRC2A	Single nucleotide variant (intron variant)	PRRC2A-related disorder	GLikely benign
Select item 3050606	NM_004638.4(PRRC2A):c.488C>T (p.Ser163Leu)	PRRC2A (S163L)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3050293	NM_004638.4(PRRC2A):c.3533CTC[1] (p.Pro1179del)	PRRC2A (P1179del)	Microsatellite	PRRC2A-related disorder	GLikely benign
Select item 3050214	NM_004638.4(PRRC2A):c.5423C>T (p.Ser1808Phe)	PRRC2A (S1808F)	Single nucleotide variant (missense variant)	PRRC2A-related disorder	GBenign
Select item 3049498	NM_004638.4(PRRC2A):c.1479C>T (p.Leu493=)	PRRC2A	Single nucleotide variant (synonymous variant)	PRRC2A-related disorder	GLikely benign

<< First< Prev

Page of 3