"Ambry Genetics"[submitter] AND "PCDH11X"[gene] - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2457141	NM_032968.5(PCDH11X):c.12G>T (p.Leu4Phe)	PCDH11X (L4F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516369	NM_032968.5(PCDH11X):c.238G>A (p.Asp80Asn)	PCDH11X (D80N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209129	NM_032968.5(PCDH11X):c.263G>T (p.Gly88Val)	PCDH11X (G88V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271814	NM_032968.5(PCDH11X):c.272T>C (p.Ile91Thr)	PCDH11X (I91T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539833	NM_032968.5(PCDH11X):c.455C>T (p.Ser152Leu)	PCDH11X (S152L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551538	NM_032968.5(PCDH11X):c.473A>G (p.Tyr158Cys)	PCDH11X (Y158C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489333	NM_032968.5(PCDH11X):c.653A>T (p.Lys218Ile)	PCDH11X (K218I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1087134	NM_032968.5(PCDH11X):c.718A>T (p.Thr240Ser)	PCDH11X (T240S)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2405216	NM_032968.5(PCDH11X):c.776C>T (p.Pro259Leu)	PCDH11X (P259L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609556	NM_032968.5(PCDH11X):c.803T>G (p.Val268Gly)	PCDH11X (V268G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304563	NM_032968.5(PCDH11X):c.1457C>T (p.Thr486Met)	PCDH11X (T486M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485342	NM_032968.5(PCDH11X):c.1657A>G (p.Asn553Asp)	PCDH11X (N553D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335829	NM_032968.5(PCDH11X):c.1658A>C (p.Asn553Thr)	PCDH11X (N553T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248515	NM_032968.5(PCDH11X):c.1850C>A (p.Thr617Asn)	PCDH11X (T617N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548995	NM_032968.5(PCDH11X):c.1877G>A (p.Arg626Gln)	PCDH11X (R626Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226449	NM_032968.5(PCDH11X):c.1958G>A (p.Arg653His)	PCDH11X (R653H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3304565	NM_032968.5(PCDH11X):c.1979C>T (p.Thr660Ile)	PCDH11X (T660I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257602	NM_032968.5(PCDH11X):c.2095A>C (p.Ile699Leu)	PCDH11X (I699L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209126	NM_032968.5(PCDH11X):c.2107A>G (p.Asn703Asp)	PCDH11X (N703D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209127	NM_032968.5(PCDH11X):c.2152G>A (p.Gly718Arg)	PCDH11X (G718R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569823	NM_032968.5(PCDH11X):c.2573A>G (p.Asn858Ser)	PCDH11X (N858S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515003	NM_032968.5(PCDH11X):c.2640C>A (p.Asn880Lys)	PCDH11X (N880K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304564	NM_032968.5(PCDH11X):c.2711C>T (p.Thr904Ile)	PCDH11X (T904I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2636350	NM_032968.5(PCDH11X):c.2834A>G (p.Gln945Arg)	PCDH11X (Q945R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2597342	NM_032968.5(PCDH11X):c.2975C>T (p.Ser992Phe)	PCDH11X (S992F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209130	NM_032968.5(PCDH11X):c.3004G>A (p.Glu1002Lys)	PCDH11X (E1002K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3209131	NM_032968.5(PCDH11X):c.3115C>T (p.Arg1039Trp)	PCDH11X (R1039W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462010	NM_032968.5(PCDH11X):c.3137C>T (p.Ala1046Val)	PCDH11X (A1046V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602925	NM_032968.5(PCDH11X):c.3230G>C (p.Ser1077Thr)	PCDH11X (S1040T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376609	NM_032968.5(PCDH11X):c.3308G>A (p.Arg1103His)	PCDH11X (R1066H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599386	NM_032968.5(PCDH11X):c.3331G>A (p.Asp1111Asn)	PCDH11X (D1074N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624294	NM_032968.5(PCDH11X):c.3346T>C (p.Phe1116Leu)	PCDH11X (F1106L +2 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2316455	NM_032968.5(PCDH11X):c.3452C>T (p.Ala1151Val)	PCDH11X (A1143V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3304562	NM_032968.5(PCDH11X):c.3491C>T (p.Ser1164Leu)	PCDH11X (S1164L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486864	NM_032968.5(PCDH11X):c.3580G>C (p.Ala1194Pro)	PCDH11X (A1194P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592570	NM_032968.5(PCDH11X):c.3614T>C (p.Ile1205Thr)	PCDH11X (I1205T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408917	NM_032968.5(PCDH11X):c.3658C>T (p.His1220Tyr)	PCDH11X (H1202Y +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3209133	NM_032968.5(PCDH11X):c.3791T>A (p.Val1264Asp)	PCDH11X (V1254D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311813	NM_032968.5(PCDH11X):c.3854G>A (p.Gly1285Asp)	PCDH11X (G1248D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2332073	NM_032968.5(PCDH11X):c.3861T>G (p.Asp1287Glu)	PCDH11X (D1287E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391463	NM_032968.5(PCDH11X):c.3935A>G (p.His1312Arg)	PCDH11X (H1312R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 41