ClinVar for Gene (Select 56143) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3239050	NM_018911.3(PCDHA8):c.2394+48G>A	PCDHA1, PCDHA2 +7 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3209536	NM_018899.6(PCDHAC2):c.710G>T (p.Arg237Leu)	PCDHA1, PCDHA10 +14 more (R237L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209535	NM_018899.6(PCDHAC2):c.314T>C (p.Ile105Thr)	PCDHA1, PCDHA10 +14 more (I105T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209534	NM_018899.6(PCDHAC2):c.2206G>A (p.Ala736Thr)	PCDHA1, PCDHA10 +14 more (A736T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209533	NM_018899.6(PCDHAC2):c.2096G>A (p.Arg699Gln)	PCDHA1, PCDHA10 +14 more (R699Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209532	NM_018899.6(PCDHAC2):c.196G>C (p.Gly66Arg)	PCDHA1, PCDHA10 +14 more (G66R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209531	NM_018899.6(PCDHAC2):c.1514C>T (p.Thr505Ile)	PCDHA13, PCDHA2 +14 more (T505I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209530	NM_018899.6(PCDHAC2):c.129G>C (p.Gln43His)	PCDHA1, PCDHA10 +14 more (Q43H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209529	NM_018898.5(PCDHAC1):c.839T>G (p.Leu280Arg)	PCDHA1, PCDHA10 +13 more (L280R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209528	NM_018898.5(PCDHAC1):c.806A>C (p.Gln269Pro)	PCDHA1, PCDHA10 +13 more (Q269P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209527	NM_018898.5(PCDHAC1):c.686A>G (p.Asn229Ser)	PCDHA1, PCDHA10 +13 more (N229S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209525	NM_018898.5(PCDHAC1):c.577C>G (p.Arg193Gly)	PCDHA1, PCDHA10 +13 more (R193G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209524	NM_018898.5(PCDHAC1):c.442G>A (p.Ala148Thr)	PCDHA1, PCDHA10 +13 more (A148T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209523	NM_018898.5(PCDHAC1):c.311C>T (p.Pro104Leu)	PCDHA1, PCDHA10 +13 more (P104L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209522	NM_018898.5(PCDHAC1):c.285G>T (p.Leu95Phe)	PCDHA1, PCDHA10 +13 more (L95F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209521	NM_018898.5(PCDHAC1):c.2291C>T (p.Ser764Phe)	PCDHA1, PCDHA10 +13 more (S764F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209519	NM_018898.5(PCDHAC1):c.1661T>A (p.Val554Asp)	PCDHA1, PCDHA10 +13 more (V554D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209518	NM_018898.5(PCDHAC1):c.1423G>A (p.Gly475Arg)	PCDHA1, PCDHA10 +13 more (G475R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209517	NM_018898.5(PCDHAC1):c.1189C>G (p.Leu397Val)	PCDHA1, PCDHA10 +13 more (L397V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209516	NM_018898.5(PCDHAC1):c.1181A>G (p.Tyr394Cys)	PCDHA1, PCDHA10 +13 more (Y394C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209515	NM_031857.2(PCDHA9):c.944C>A (p.Ala315Glu)	PCDHA1, PCDHA2 +8 more (A315E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209514	NM_031857.2(PCDHA9):c.404C>A (p.Ala135Glu)	PCDHA1, PCDHA2 +8 more (A135E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209513	NM_031857.2(PCDHA9):c.2380G>A (p.Asp794Asn)	PCDHA1, PCDHA2 +8 more (D794N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209512	NM_031857.2(PCDHA9):c.2185G>A (p.Glu729Lys)	PCDHA1, PCDHA2 +8 more (E729K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209511	NM_031857.2(PCDHA9):c.211C>T (p.Arg71Cys)	PCDHA1, PCDHA2 +8 more (R71C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209510	NM_031857.2(PCDHA9):c.2015G>C (p.Ser672Thr)	PCDHA1, PCDHA2 +8 more (S672T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209509	NM_031857.2(PCDHA9):c.1915G>C (p.Glu639Gln)	PCDHA1, PCDHA2 +8 more (E639Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209508	NM_031857.2(PCDHA9):c.1851C>A (p.Ser617Arg)	PCDHA1, PCDHA2 +8 more (S617R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209507	NM_031857.2(PCDHA9):c.1820T>G (p.Leu607Arg)	PCDHA1, PCDHA2 +8 more (L607R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209506	NM_031857.2(PCDHA9):c.1798G>A (p.Asp600Asn)	PCDHA1, PCDHA2 +8 more (D600N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209505	NM_031857.2(PCDHA9):c.1717A>C (p.Thr573Pro)	PCDHA1, PCDHA2 +8 more (T573P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209504	NM_031857.2(PCDHA9):c.163G>C (p.Glu55Gln)	PCDHA1, PCDHA2 +8 more (E55Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209503	NM_031857.2(PCDHA9):c.1615G>A (p.Asp539Asn)	PCDHA1, PCDHA2 +8 more (D539N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209502	NM_031857.2(PCDHA9):c.1543G>A (p.Gly515Ser)	PCDHA1, PCDHA2 +8 more (G515S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209501	NM_031857.2(PCDHA9):c.1495T>G (p.Leu499Val)	PCDHA1, PCDHA2 +8 more (L499V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3209500	NM_031857.2(PCDHA9):c.1490G>T (p.Arg497Leu)	PCDHA1, PCDHA2 +8 more (R497L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209499	NM_031857.2(PCDHA9):c.1348G>A (p.Asp450Asn)	PCDHA1, PCDHA2 +8 more (D450N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209498	NM_031857.2(PCDHA9):c.1222G>C (p.Val408Leu)	PCDHA1, PCDHA2 +8 more (V408L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209497	NM_031857.2(PCDHA9):c.1198A>C (p.Thr400Pro)	PCDHA1, PCDHA2 +8 more (T400P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209496	NM_031857.2(PCDHA9):c.1102G>T (p.Val368Phe)	PCDHA1, PCDHA2 +8 more (V368F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209495	NM_031857.2(PCDHA9):c.1094T>C (p.Leu365Pro)	PCDHA1, PCDHA2 +8 more (L365P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209494	NM_031857.2(PCDHA9):c.1052C>T (p.Thr351Ile)	PCDHA1, PCDHA2 +8 more (T351I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3209493	NM_018911.3(PCDHA8):c.965C>T (p.Ala322Val)	PCDHA1, PCDHA2 +7 more (A322V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209492	NM_018911.3(PCDHA8):c.718C>T (p.Pro240Ser)	PCDHA1, PCDHA2 +7 more (P240S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209491	NM_018911.3(PCDHA8):c.38G>T (p.Arg13Leu)	PCDHA1, PCDHA2 +7 more (R13L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209490	NM_018911.3(PCDHA8):c.352C>T (p.His118Tyr)	PCDHA1, PCDHA2 +7 more (H118Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209489	NM_018911.3(PCDHA8):c.239A>G (p.Gln80Arg)	PCDHA1, PCDHA2 +7 more (Q80R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209488	NM_018911.3(PCDHA8):c.2367A>T (p.Gln789His)	PCDHA1, PCDHA2 +7 more (Q789H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209487	NM_018911.3(PCDHA8):c.2168G>T (p.Cys723Phe)	PCDHA1, PCDHA2 +7 more (C723F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209486	NM_018911.3(PCDHA8):c.2150T>C (p.Leu717Pro)	PCDHA1, PCDHA2 +7 more (L717P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209485	NM_018911.3(PCDHA8):c.2093T>G (p.Val698Gly)	PCDHA1, PCDHA2 +7 more (V698G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209484	NM_018911.3(PCDHA8):c.2065C>A (p.Pro689Thr)	PCDHA1, PCDHA2 +7 more (P689T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209483	NM_018911.3(PCDHA8):c.1874G>T (p.Gly625Val)	PCDHA1, PCDHA2 +7 more (G625V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209482	NM_018911.3(PCDHA8):c.1706G>C (p.Arg569Pro)	PCDHA1, PCDHA2 +7 more (R569P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209481	NM_018911.3(PCDHA8):c.1688C>T (p.Pro563Leu)	PCDHA1, PCDHA2 +7 more (P563L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209480	NM_018911.3(PCDHA8):c.1608C>G (p.Ser536Arg)	PCDHA1, PCDHA2 +7 more (S536R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209479	NM_018911.3(PCDHA8):c.1532A>C (p.His511Pro)	PCDHA1, PCDHA2 +7 more (H511P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209478	NM_018911.3(PCDHA8):c.1517G>A (p.Ser506Asn)	PCDHA1, PCDHA2 +7 more (S506N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209476	NM_018911.3(PCDHA8):c.1417C>T (p.His473Tyr)	PCDHA1, PCDHA2 +7 more (H473Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209475	NM_018911.3(PCDHA8):c.1390G>C (p.Val464Leu)	PCDHA1, PCDHA2 +7 more (V464L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209474	NM_018911.3(PCDHA8):c.1376A>T (p.Glu459Val)	PCDHA1, PCDHA2 +7 more (E459V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209473	NM_018911.3(PCDHA8):c.1202T>A (p.Phe401Tyr)	PCDHA1, PCDHA2 +7 more (F401Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209472	NM_018910.3(PCDHA7):c.923T>C (p.Met308Thr)	PCDHA1, PCDHA2 +6 more (M308T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209471	NM_018910.3(PCDHA7):c.899G>T (p.Gly300Val)	PCDHA1, PCDHA2 +6 more (G300V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209470	NM_018910.3(PCDHA7):c.254T>C (p.Phe85Ser)	PCDHA1, PCDHA2 +6 more (F85S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209469	NM_018910.3(PCDHA7):c.2117C>A (p.Ala706Glu)	PCDHA1, PCDHA2 +6 more (A706E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209468	NM_018910.3(PCDHA7):c.2016C>A (p.Ser672Arg)	PCDHA1, PCDHA2 +6 more (S672R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209467	NM_018910.3(PCDHA7):c.1833G>C (p.Leu611Phe)	PCDHA1, PCDHA2 +6 more (L611F)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3209466	NM_018910.3(PCDHA7):c.178G>A (p.Val60Met)	PCDHA1, PCDHA2 +6 more (V60M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209465	NM_018910.3(PCDHA7):c.1784G>T (p.Arg595Leu)	PCDHA1, PCDHA2 +6 more (R595L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209464	NM_018910.3(PCDHA7):c.1712G>A (p.Gly571Asp)	PCDHA1, PCDHA2 +6 more (G571D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209462	NM_018910.3(PCDHA7):c.1685C>T (p.Ala562Val)	PCDHA1, PCDHA2 +6 more (A562V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209461	NM_018910.3(PCDHA7):c.1592T>G (p.Leu531Trp)	PCDHA1, PCDHA2 +6 more (L531W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209460	NM_018910.3(PCDHA7):c.1508C>T (p.Ala503Val)	PCDHA1, PCDHA2 +6 more (A503V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209459	NM_018910.3(PCDHA7):c.1185C>G (p.Phe395Leu)	PCDHA1, PCDHA2 +6 more (F395L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209458	NM_018910.3(PCDHA7):c.1147G>C (p.Gly383Arg)	PCDHA1, PCDHA2 +6 more (G383R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209457	NM_018909.4(PCDHA6):c.925G>C (p.Asp309His)	PCDHA1, PCDHA2 +5 more (D309H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209456	NM_018909.4(PCDHA6):c.904A>G (p.Ile302Val)	PCDHA1, PCDHA2 +5 more (I302V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209455	NM_018909.4(PCDHA6):c.849C>G (p.Ser283Arg)	PCDHA1, PCDHA2 +5 more (S283R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209454	NM_018909.4(PCDHA6):c.781G>A (p.Val261Ile)	PCDHA1, PCDHA2 +5 more (V261I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209453	NM_018909.4(PCDHA6):c.718C>T (p.Pro240Ser)	PCDHA1, PCDHA2 +5 more (P240S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209452	NM_018909.4(PCDHA6):c.536G>A (p.Gly179Glu)	PCDHA1, PCDHA2 +5 more (G179E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209451	NM_018909.4(PCDHA6):c.293G>A (p.Arg98Gln)	PCDHA1, PCDHA2 +5 more (R98Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209450	NM_018909.4(PCDHA6):c.243T>G (p.Asn81Lys)	PCDHA1, PCDHA2 +5 more (N81K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209449	NM_018909.4(PCDHA6):c.2384A>G (p.His795Arg)	PCDHA1, PCDHA2 +5 more (H795R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209448	NM_018909.4(PCDHA6):c.2297A>G (p.Lys766Arg)	PCDHA1, PCDHA2 +5 more (K766R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209447	NM_018909.4(PCDHA6):c.1922A>G (p.Asp641Gly)	PCDHA1, PCDHA2 +5 more (D641G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209446	NM_018909.4(PCDHA6):c.190T>G (p.Phe64Val)	PCDHA1, PCDHA2 +5 more (F64V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209444	NM_018909.4(PCDHA6):c.1748G>A (p.Arg583Gln)	PCDHA1, PCDHA2 +5 more (R583Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209443	NM_018909.4(PCDHA6):c.1555G>C (p.Ala519Pro)	PCDHA1, PCDHA2 +5 more (A519P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209442	NM_018909.4(PCDHA6):c.1466T>C (p.Leu489Pro)	PCDHA1, PCDHA2 +5 more (L489P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209441	NM_018909.4(PCDHA6):c.1443C>G (p.Asp481Glu)	PCDHA1, PCDHA2 +5 more (D481E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209440	NM_018909.4(PCDHA6):c.1342A>G (p.Met448Val)	PCDHA1, PCDHA2 +5 more (M448V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3209439	NM_018909.4(PCDHA6):c.1313C>T (p.Thr438Ile)	PCDHA1, PCDHA2 +5 more (T438I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209438	NM_018909.4(PCDHA6):c.1292G>C (p.Gly431Ala)	PCDHA1, PCDHA2 +5 more (G431A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209437	NM_018908.3(PCDHA5):c.977C>A (p.Thr326Lys)	PCDHA1, PCDHA2 +4 more (T326K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209436	NM_018908.3(PCDHA5):c.838T>C (p.Phe280Leu)	PCDHA1, PCDHA2 +4 more (F280L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209435	NM_018908.3(PCDHA5):c.417A>C (p.Leu139Phe)	PCDHA1, PCDHA2 +4 more (L139F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209434	NM_018908.3(PCDHA5):c.292A>T (p.Arg98Trp)	PCDHA1, PCDHA2 +4 more (R98W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209433	NM_018908.3(PCDHA5):c.266T>G (p.Ile89Ser)	PCDHA1, PCDHA2 +4 more (I89S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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