ClinVar for Gene (Select 56106) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3415645	NM_018929.3(PCDHGC5):c.754C>A (p.Pro252Thr)	PCDHG@, PCDHGA1 +21 more (P252T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415644	NM_018929.3(PCDHGC5):c.2309A>T (p.Gln770Leu)	PCDHG@, PCDHGA1 +21 more (Q770L)	Single nucleotide variant (intron variant +1 more)	not specified	GUncertain significance
Select item 3415643	NM_018929.3(PCDHGC5):c.1750C>T (p.Pro584Ser)	PCDHG@, PCDHGA1 +21 more (P584S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415642	NM_018929.3(PCDHGC5):c.1124G>A (p.Arg375Gln)	PCDHG@, PCDHGA1 +21 more (R375Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415641	NM_018929.3(PCDHGC5):c.238A>G (p.Met80Val)	PCDHG@, PCDHGA1 +21 more (M80V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3415640	NM_018929.3(PCDHGC5):c.1172C>A (p.Pro391Gln)	PCDHG@, PCDHGA1 +21 more (P391Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415639	NM_018928.3(PCDHGC4):c.181G>C (p.Ala61Pro)	PCDHG@, PCDHGA1 +20 more (A61P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415637	NM_018928.3(PCDHGC4):c.1949G>A (p.Ser650Asn)	PCDHG@, PCDHGA1 +20 more (S650N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415636	NM_018928.3(PCDHGC4):c.643G>T (p.Val215Phe)	PCDHG@, PCDHGA1 +20 more (V215F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415635	NM_018928.3(PCDHGC4):c.2409C>G (p.Ser803Arg)	PCDHG@, PCDHGA1 +20 more (S803R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415634	NM_018928.3(PCDHGC4):c.1517C>G (p.Ser506Cys)	PCDHG@, PCDHGA1 +20 more (S506C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415633	NM_018928.3(PCDHGC4):c.2285T>C (p.Phe762Ser)	PCDHG@, PCDHGA1 +20 more (F762S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415632	NM_018928.3(PCDHGC4):c.1066C>G (p.Leu356Val)	PCDHG@, PCDHGA1 +20 more (L356V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415631	NM_018928.3(PCDHGC4):c.1253A>G (p.Lys418Arg)	PCDHG@, PCDHGA1 +20 more (K418R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415630	NM_018928.3(PCDHGC4):c.566G>A (p.Ser189Asn)	PCDHG@, PCDHGA1 +20 more (S189N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415629	NM_018928.3(PCDHGC4):c.829G>A (p.Val277Ile)	PCDHG@, PCDHGA1 +20 more (V277I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415628	NM_018928.3(PCDHGC4):c.1613G>A (p.Arg538Gln)	PCDHG@, PCDHGA1 +20 more (R538Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3415626	NM_002588.4(PCDHGC3):c.2425G>A (p.Gly809Arg)	PCDHG@, PCDHGA1 +19 more (G809R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415625	NM_002588.4(PCDHGC3):c.1655G>C (p.Ser552Thr)	PCDHG@, PCDHGA1 +19 more (S552T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415624	NM_002588.4(PCDHGC3):c.839T>C (p.Ile280Thr)	PCDHG@, PCDHGA1 +19 more (I280T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415623	NM_002588.4(PCDHGC3):c.875G>A (p.Arg292Gln)	PCDHG@, PCDHGA1 +19 more (R292Q)	Single nucleotide variant (intron variant +1 more)	not specified	GUncertain significance
Select item 3415622	NM_002588.4(PCDHGC3):c.2180A>G (p.Tyr727Cys)	PCDHG@, PCDHGA1 +19 more (Y727C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415621	NM_002588.4(PCDHGC3):c.2186C>T (p.Ala729Val)	PCDHG@, PCDHGA1 +19 more (A729V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415620	NM_002588.4(PCDHGC3):c.464C>T (p.Pro155Leu)	PCDHG@, PCDHGA1 +19 more (P155L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415619	NM_002588.4(PCDHGC3):c.2219C>T (p.Pro740Leu)	PCDHG@, PCDHGA1 +19 more (P740L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415618	NM_002588.4(PCDHGC3):c.1294G>A (p.Ala432Thr)	PCDHG@, PCDHGA1 +19 more (A432T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415616	NM_002588.4(PCDHGC3):c.1388A>T (p.Asp463Val)	PCDHG@, PCDHGA1 +19 more (D463V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415615	NM_002588.4(PCDHGC3):c.1981A>G (p.Thr661Ala)	PCDHG@, PCDHGA1 +19 more (T661A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415614	NM_002588.4(PCDHGC3):c.787G>A (p.Val263Met)	PCDHG@, PCDHGA1 +19 more (V263M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415613	NM_002588.4(PCDHGC3):c.224G>A (p.Arg75Lys)	PCDHG@, PCDHGA1 +19 more (R75K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415612	NM_018927.4(PCDHGB7):c.2230A>G (p.Ser744Gly)	PCDHG@, PCDHGA1 +16 more (S744G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415611	NM_018927.4(PCDHGB7):c.541G>C (p.Val181Leu)	PCDHG@, PCDHGA1 +16 more (V181L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415610	NM_018927.4(PCDHGB7):c.737T>C (p.Val246Ala)	PCDHG@, PCDHGA1 +16 more (V246A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415609	NM_018927.4(PCDHGB7):c.1093G>C (p.Val365Leu)	PCDHG@, PCDHGA1 +16 more (V365L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415608	NM_018927.4(PCDHGB7):c.2275G>A (p.Asp759Asn)	PCDHG@, PCDHGA1 +16 more (D759N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415607	NM_018927.4(PCDHGB7):c.762C>A (p.Asp254Glu)	PCDHG@, PCDHGA1 +16 more (D254E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415606	NM_018927.4(PCDHGB7):c.1574T>C (p.Leu525Pro)	PCDHG@, PCDHGA1 +16 more (L525P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415605	NM_018927.4(PCDHGB7):c.733G>A (p.Asp245Asn)	PCDHG@, PCDHGA1 +16 more (D245N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415604	NM_018927.4(PCDHGB7):c.287G>A (p.Cys96Tyr)	PCDHG@, PCDHGA1 +16 more (C96Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415603	NM_018927.4(PCDHGB7):c.1945G>A (p.Gly649Arg)	PCDHG@, PCDHGA1 +16 more (G649R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415602	NM_018927.4(PCDHGB7):c.2218C>T (p.Pro740Ser)	PCDHG@, PCDHGA1 +16 more (P740S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415378	NM_003735.3(PCDHGA12):c.1786A>G (p.Arg596Gly)	PCDHG@, PCDHGA1 +18 more (R596G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415377	NM_003735.3(PCDHGA12):c.1871G>A (p.Gly624Asp)	PCDHG@, PCDHGA1 +18 more (G624D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415376	NM_003735.3(PCDHGA12):c.691A>G (p.Met231Val)	PCDHG@, PCDHGA1 +18 more (M231V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415375	NM_003735.3(PCDHGA12):c.151G>A (p.Asp51Asn)	PCDHG@, PCDHGA1 +18 more (D51N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415374	NM_003735.3(PCDHGA12):c.1973T>G (p.Val658Gly)	PCDHG@, PCDHGA1 +18 more (V658G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415373	NM_003735.3(PCDHGA12):c.1023C>G (p.Asn341Lys)	PCDHG@, PCDHGA1 +18 more (N341K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415372	NM_003735.3(PCDHGA12):c.1279C>T (p.Arg427Trp)	PCDHG@, PCDHGA1 +18 more (R427W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415371	NM_003735.3(PCDHGA12):c.701A>T (p.Asp234Val)	PCDHG@, PCDHGA1 +18 more (D234V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415370	NM_003735.3(PCDHGA12):c.2300A>G (p.His767Arg)	PCDHG@, PCDHGA1 +18 more (H767R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415369	NM_003735.3(PCDHGA12):c.1432G>C (p.Asp478His)	PCDHG@, PCDHGA1 +18 more (D478H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415368	NM_003735.3(PCDHGA12):c.2383G>T (p.Gly795Cys)	PCDHG@, PCDHGA1 +18 more (G795C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415367	NM_003735.3(PCDHGA12):c.86C>T (p.Thr29Ile)	PCDHG@, PCDHGA1 +18 more (T29I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415366	NM_003735.3(PCDHGA12):c.2032C>T (p.Leu678Phe)	PCDHG@, PCDHGA1 +18 more (L678F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415365	NM_003735.3(PCDHGA12):c.1444G>A (p.Glu482Lys)	PCDHG@, PCDHGA1 +18 more (E482K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415364	NM_003735.3(PCDHGA12):c.1886C>A (p.Ala629Glu)	PCDHG@, PCDHGA1 +18 more (A629E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415363	NM_003735.3(PCDHGA12):c.1523A>G (p.Asn508Ser)	PCDHG@, PCDHGA1 +18 more (N508S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415361	NM_018914.3(PCDHGA11):c.1187A>T (p.Glu396Val)	PCDHG@, PCDHGA1 +17 more (E396V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415360	NM_018914.3(PCDHGA11):c.531T>G (p.Asn177Lys)	PCDHG@, PCDHGA1 +17 more (N177K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415359	NM_018914.3(PCDHGA11):c.1886C>G (p.Thr629Arg)	PCDHG@, PCDHGA1 +17 more (T629R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415358	NM_018914.3(PCDHGA11):c.197G>T (p.Arg66Leu)	PCDHG@, PCDHGA1 +17 more (R66L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415357	NM_018914.3(PCDHGA11):c.1624C>T (p.Pro542Ser)	PCDHG@, PCDHGA1 +17 more (P542S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415356	NM_018914.3(PCDHGA11):c.674G>A (p.Gly225Asp)	PCDHG@, PCDHGA1 +17 more (G225D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415355	NM_018914.3(PCDHGA11):c.1525A>C (p.Asn509His)	PCDHG@, PCDHGA1 +17 more (N509H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415354	NM_018914.3(PCDHGA11):c.2173C>A (p.Leu725Met)	PCDHG@, PCDHGA1 +17 more (L725M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415353	NM_018914.3(PCDHGA11):c.1568A>G (p.Tyr523Cys)	PCDHG@, PCDHGA1 +17 more (Y523C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415352	NM_018914.3(PCDHGA11):c.491G>A (p.Gly164Asp)	PCDHG@, PCDHGA1 +17 more (G164D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415351	NM_018914.3(PCDHGA11):c.1903G>A (p.Asp635Asn)	PCDHG@, PCDHGA1 +17 more (D635N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415350	NM_018914.3(PCDHGA11):c.121G>C (p.Glu41Gln)	PCDHG@, PCDHGA1 +17 more (E41Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415349	NM_018913.3(PCDHGA10):c.1544C>T (p.Thr515Ile)	PCDHG@, PCDHGA1 +15 more (T515I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415348	NM_018913.3(PCDHGA10):c.1942G>T (p.Val648Leu)	PCDHG@, PCDHGA1 +15 more (V648L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415347	NM_018913.3(PCDHGA10):c.130G>A (p.Glu44Lys)	PCDHG@, PCDHGA1 +15 more (E44K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415346	NM_018913.3(PCDHGA10):c.1252C>G (p.Gln418Glu)	PCDHG@, PCDHGA1 +15 more (Q418E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415345	NM_018913.3(PCDHGA10):c.223A>G (p.Arg75Gly)	PCDHG@, PCDHGA1 +15 more (R75G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415344	NM_018913.3(PCDHGA10):c.1469A>C (p.Gln490Pro)	PCDHG@, PCDHGA1 +15 more (Q490P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415343	NM_018913.3(PCDHGA10):c.845C>T (p.Thr282Ile)	PCDHG@, PCDHGA1 +15 more (T282I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415342	NM_018913.3(PCDHGA10):c.589G>A (p.Glu197Lys)	PCDHG@, PCDHGA1 +15 more (E197K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415341	NM_018913.3(PCDHGA10):c.713A>G (p.Asp238Gly)	PCDHG@, PCDHGA1 +15 more (D238G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415340	NM_018913.3(PCDHGA10):c.1895C>T (p.Thr632Met)	PCDHG@, PCDHGA1 +15 more (T632M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3415339	NM_018913.3(PCDHGA10):c.2044T>C (p.Phe682Leu)	PCDHG@, PCDHGA1 +15 more (F682L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3415338	NM_018913.3(PCDHGA10):c.1972C>A (p.Leu658Ile)	PCDHG@, PCDHGA1 +15 more (L658I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305075	NM_018929.3(PCDHGC5):c.1469C>T (p.Thr490Ile)	PCDHG@, PCDHGA1 +21 more (T490I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305074	NM_018929.3(PCDHGC5):c.1309C>T (p.His437Tyr)	PCDHG@, PCDHGA1 +21 more (H437Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305073	NM_018929.3(PCDHGC5):c.2201A>G (p.Gln734Arg)	PCDHG@, PCDHGA1 +21 more (Q734R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305072	NM_018929.3(PCDHGC5):c.1130G>C (p.Arg377Pro)	PCDHG@, PCDHGA1 +21 more (R377P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305070	NM_018929.3(PCDHGC5):c.910G>A (p.Val304Met)	PCDHG@, PCDHGA1 +21 more (V304M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305069	NM_018928.3(PCDHGC4):c.1700G>A (p.Arg567His)	PCDHG@, PCDHGA1 +20 more (R567H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3305068	NM_018928.3(PCDHGC4):c.2219G>C (p.Arg740Thr)	PCDHG@, PCDHGA1 +20 more (R740T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3305067	NM_018928.3(PCDHGC4):c.1960C>T (p.Pro654Ser)	PCDHG@, PCDHGA1 +20 more (P654S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3305066	NM_018928.3(PCDHGC4):c.919C>A (p.Pro307Thr)	PCDHG@, PCDHGA1 +20 more (P307T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3305065	NM_018928.3(PCDHGC4):c.1081G>A (p.Glu361Lys)	PCDHG@, PCDHGA1 +20 more (E361K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3305064	NM_018928.3(PCDHGC4):c.1955G>A (p.Ser652Asn)	PCDHG@, PCDHGA1 +20 more (S652N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3305063	NM_018928.3(PCDHGC4):c.1129C>A (p.Pro377Thr)	PCDHG@, PCDHGA1 +20 more (P377T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3305062	NM_002588.4(PCDHGC3):c.1273C>T (p.Leu425Phe)	PCDHG@, PCDHGA1 +19 more (L425F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305061	NM_002588.4(PCDHGC3):c.268G>A (p.Asp90Asn)	PCDHG@, PCDHGA1 +19 more (D90N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305059	NM_002588.4(PCDHGC3):c.1307C>T (p.Ser436Phe)	PCDHGA4, PCDHGA5 +19 more (S436F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305058	NM_002588.4(PCDHGC3):c.2143T>A (p.Phe715Ile)	PCDHG@, PCDHGA1 +19 more (F715I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305057	NM_018927.4(PCDHGB7):c.226A>C (p.Ser76Arg)	PCDHG@, PCDHGA1 +16 more (S76R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305056	NM_018927.4(PCDHGB7):c.385C>T (p.His129Tyr)	PCDHG@, PCDHGA1 +16 more (H129Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305055	NM_018927.4(PCDHGB7):c.1513G>A (p.Val505Met)	PCDHG@, PCDHGA1 +16 more (V505M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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