Related gene-specific medical variations for Gene (Select 56136) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044886	NM_018904.3(PCDHA13):c.2802C>T (p.Thr934=)	PCDHA1, PCDHA10 +15 more	Single nucleotide variant (synonymous variant)	PCDHA13-related condition	GBenign
Select item 3044804	NM_018904.3(PCDHA13):c.2543-9_2543-8del	PCDHA1, PCDHA10 +15 more	Deletion (intron variant)	PCDHA13-related condition	GLikely benign
Select item 2673031	NM_018899.6(PCDHAC2):c.1911G>A (p.Leu637=)	PCDHA1, PCDHA10 +14 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655805	NM_018899.6(PCDHAC2):c.2460G>A (p.Ser820=)	PCDHA1, PCDHA10 +14 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655804	NM_018899.6(PCDHAC2):c.1161C>G (p.Leu387=)	PCDHA1, PCDHA10 +14 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655803	NM_018899.6(PCDHAC2):c.480G>T (p.Ser160=)	PCDHA1, PCDHA10 +14 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655802	NM_018898.5(PCDHAC1):c.1671T>C (p.Phe557=)	PCDHA9, PCDHA@ +13 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655801	NM_018904.3(PCDHA13):c.2202G>A (p.Pro734=)	PCDHA1, PCDHA10 +12 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655800	NM_018904.3(PCDHA13):c.2164C>A (p.Arg722=)	PCDHA1, PCDHA10 +12 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655799	NM_018907.4(PCDHA4):c.2385+74492C>A	PCDHA1, PCDHA10 +12 more (A599D)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2655798	NM_018902.5(PCDHA11):c.2391+12410G>A	PCDHA1, PCDHA10 +12 more (G546S)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2655797	NM_018904.3(PCDHA13):c.1428G>C (p.Thr476=)	PCDHA1, PCDHA10 +12 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655796	NM_018904.3(PCDHA13):c.292C>A (p.Arg98=)	PCDHA2, PCDHA1 +12 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2622061	NM_018898.5(PCDHAC1):c.1771G>T (p.Gly591Cys)	PCDHA2, PCDHA3 +13 more (G591C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2621776	NM_018904.3(PCDHA13):c.849G>T (p.Arg283Ser)	PCDHA1, PCDHA10 +12 more (R283S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2620601	NM_018904.3(PCDHA13):c.2141C>G (p.Thr714Arg)	PCDHA13, PCDHA2 +12 more (T714R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2620600	NM_018904.3(PCDHA13):c.182C>A (p.Pro61Gln)	PCDHA1, PCDHA10 +12 more (P61Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2619201	NM_018899.6(PCDHAC2):c.2207C>A (p.Ala736Glu)	PCDHA1, PCDHA13 +14 more (A736E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2616930	NM_018904.3(PCDHA13):c.1955A>G (p.Lys652Arg)	PCDHA9, PCDHA@ +12 more (K652R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2616131	NM_018898.5(PCDHAC1):c.604G>A (p.Val202Met)	PCDHA1, PCDHA10 +13 more (V202M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2612504	NM_018898.5(PCDHAC1):c.1195A>T (p.Ile399Phe)	PCDHA6, PCDHA7 +13 more (I399F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2612393	NM_018904.3(PCDHA13):c.850C>G (p.Pro284Ala)	PCDHA@, PCDHA1 +12 more (P284A)	Single nucleotide variant (intron variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2610865	NM_018904.3(PCDHA13):c.140G>C (p.Arg47Pro)	PCDHA6, PCDHA7 +12 more (R47P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2610172	NM_018904.3(PCDHA13):c.286T>G (p.Cys96Gly)	PCDHA1, PCDHA10 +12 more (C96G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2609940	NM_018904.3(PCDHA13):c.1010T>C (p.Leu337Ser)	PCDHA1, PCDHA10 +12 more (L337S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2608214	NM_018899.6(PCDHAC2):c.1582A>G (p.Ser528Gly)	PCDHA1, PCDHA10 +14 more (S528G)	Single nucleotide variant (intron variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2607186	NM_018904.3(PCDHA13):c.719C>T (p.Pro240Leu)	PCDHA4, PCDHA5 +12 more (P240L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2606714	NM_018898.5(PCDHAC1):c.1735T>G (p.Leu579Val)	PCDHA11, PCDHA12 +13 more (L579V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2605385	NM_018898.5(PCDHAC1):c.1067G>A (p.Gly356Asp)	PCDHA10, PCDHA11 +13 more (G356D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2605063	NM_018898.5(PCDHAC1):c.1915C>T (p.Arg639Trp)	PCDHA13, PCDHA2 +13 more (R639W)	Single nucleotide variant (intron variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2600783	NM_018904.3(PCDHA13):c.2134G>T (p.Val712Leu)	PCDHA5, PCDHA8 +12 more (V712L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2600086	NM_018898.5(PCDHAC1):c.856G>A (p.Val286Met)	PCDHA6, PCDHA7 +13 more (V286M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2599953	NM_018898.5(PCDHAC1):c.989T>C (p.Val330Ala)	PCDHA13, PCDHA2 +13 more (V330A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2597521	NM_018904.3(PCDHA13):c.1444G>A (p.Ala482Thr)	PCDHA1, PCDHA10 +12 more (A482T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2588412	NM_018899.6(PCDHAC2):c.2197C>T (p.Arg733Cys)	PCDHA1, PCDHA10 +14 more (R733C)	Single nucleotide variant (intron variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2569460	NM_018904.3(PCDHA13):c.1440G>C (p.Gln480His)	PCDHA1, PCDHA10 +12 more (Q480H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2569459	NM_018904.3(PCDHA13):c.1439A>G (p.Gln480Arg)	PCDHA1, PCDHA10 +12 more (Q480R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2569458	NM_018904.3(PCDHA13):c.1405C>G (p.Pro469Ala)	PCDHA1, PCDHA10 +12 more (P469A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2569457	NM_018904.3(PCDHA13):c.1361C>T (p.Ala454Val)	PCDHA1, PCDHA10 +12 more (A454V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2569456	NM_018904.3(PCDHA13):c.1331G>A (p.Gly444Glu)	PCDHA1, PCDHA10 +12 more (G444E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2569455	NM_018904.3(PCDHA13):c.1318A>C (p.Ser440Arg)	PCDHA1, PCDHA10 +12 more (S440R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2569454	NM_018904.3(PCDHA13):c.1277C>G (p.Thr426Ser)	PCDHA1, PCDHA10 +12 more (T426S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2569453	NM_018904.3(PCDHA13):c.1255T>G (p.Ser419Ala)	PCDHA1, PCDHA10 +12 more (S419A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2569451	NM_018904.3(PCDHA13):c.1234G>A (p.Ala412Thr)	PCDHA1, PCDHA10 +12 more (A412T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2569450	NM_018904.3(PCDHA13):c.1231A>G (p.Ser411Gly)	PCDHA1, PCDHA10 +12 more (S411G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2546901	NM_018898.5(PCDHAC1):c.1208T>A (p.Leu403Gln)	PCDHA1, PCDHA10 +13 more (L403Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2546881	NM_018904.3(PCDHA13):c.804T>A (p.Asp268Glu)	PCDHA10, PCDHA11 +12 more (D268E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2543426	NM_018904.3(PCDHA13):c.2048C>G (p.Ser683Trp)	PCDHA1, PCDHA10 +12 more (S683W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2534912	NM_018904.3(PCDHA13):c.1444G>C (p.Ala482Pro)	PCDHA1, PCDHA10 +12 more (A482P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2534422	NM_018904.3(PCDHA13):c.1553A>T (p.Tyr518Phe)	PCDHA1, PCDHA10 +12 more (Y518F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2534421	NM_018904.3(PCDHA13):c.1546A>C (p.Lys516Gln)	PCDHA1, PCDHA10 +12 more (K516Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2534420	NM_018904.3(PCDHA13):c.1471T>G (p.Ser491Ala)	PCDHA11, PCDHA12 +12 more (S491A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2534418	NM_018904.3(PCDHA13):c.1466T>G (p.Leu489Arg)	PCDHA1, PCDHA10 +12 more (L489R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2528641	NM_018898.5(PCDHAC1):c.1459G>A (p.Val487Ile)	PCDHA1, PCDHA4 +13 more (V487I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2524848	NM_018904.3(PCDHA13):c.1337C>G (p.Ala446Gly)	PCDHA1, PCDHA10 +12 more (A446G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2516470	NM_018904.3(PCDHA13):c.128C>A (p.Thr43Asn)	PCDHA1, PCDHA10 +12 more (T43N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2495327	NM_018899.6(PCDHAC2):c.776A>G (p.Gln259Arg)	PCDHA2, PCDHA7 +14 more (Q259R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2493417	NM_018898.5(PCDHAC1):c.1999T>A (p.Phe667Ile)	PCDHA6, PCDHA9 +13 more (F667I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2492323	NM_018898.5(PCDHAC1):c.2018C>G (p.Pro673Arg)	PCDHA3, PCDHA4 +13 more (P673R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2491880	NM_018898.5(PCDHAC1):c.517A>G (p.Met173Val)	PCDHA1, PCDHA10 +13 more (M173V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2489823	NM_018898.5(PCDHAC1):c.1123G>C (p.Val375Leu)	PCDHA1, PCDHA10 +13 more (V375L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2488210	NM_018904.3(PCDHA13):c.1190T>G (p.Leu397Arg)	PCDHA12, PCDHA1 +12 more (L397R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2488209	NM_018904.3(PCDHA13):c.1189C>A (p.Leu397Met)	PCDHA6, PCDHA8 +12 more (L397M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2483045	NM_018904.3(PCDHA13):c.151G>A (p.Asp51Asn)	PCDHA1, PCDHA10 +12 more (D51N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2473674	NM_018904.3(PCDHA13):c.2090A>G (p.Asn697Ser)	PCDHA4, PCDHA5 +12 more (N697S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2394566	NM_018898.5(PCDHAC1):c.540C>G (p.Ser180Arg)	PCDHA12, PCDHA8 +13 more (S180R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2394329	NM_018904.3(PCDHA13):c.14G>T (p.Trp5Leu)	PCDHA9, PCDHA11 +12 more (W5L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2393841	NM_018898.5(PCDHAC1):c.1222A>C (p.Ile408Leu)	PCDHA7, PCDHA5 +13 more (I408L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2390226	NM_018899.6(PCDHAC2):c.1292G>A (p.Arg431Gln)	PCDHA1, PCDHA2 +14 more (R431Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2388925	NM_018898.5(PCDHAC1):c.187G>C (p.Glu63Gln)	PCDHA@, PCDHA1 +13 more (E63Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2381300	NM_018899.6(PCDHAC2):c.1349C>T (p.Thr450Ile)	PCDHAC2, PCDHA5 +14 more (T450I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2377878	NM_018904.3(PCDHA13):c.1682A>T (p.Asn561Ile)	PCDHA9, PCDHA11 +12 more (N561I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2377663	NM_018898.5(PCDHAC1):c.973A>G (p.Lys325Glu)	PCDHA3, PCDHA5 +13 more (K325E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2364742	NM_018899.6(PCDHAC2):c.2252G>A (p.Arg751Lys)	PCDHA8, PCDHA1 +14 more (R751K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2363813	NM_018899.6(PCDHAC2):c.2038G>T (p.Val680Leu)	PCDHA6, PCDHA9 +14 more (V680L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2349480	NM_018898.5(PCDHAC1):c.452A>G (p.Asp151Gly)	PCDHA2, PCDHAC1 +13 more (D151G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2341402	NM_018904.3(PCDHA13):c.1396G>A (p.Glu466Lys)	PCDHA6, PCDHA1 +12 more (E466K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2338603	NM_018898.5(PCDHAC1):c.1165G>T (p.Ala389Ser)	PCDHA13, PCDHA8 +13 more (A389S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2335013	NM_018899.6(PCDHAC2):c.2212G>T (p.Gly738Cys)	PCDHA13, PCDHA9 +14 more (G738C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2334108	NM_018899.6(PCDHAC2):c.1589G>C (p.Ser530Thr)	PCDHA12, PCDHA1 +14 more (S530T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2331542	NM_018899.6(PCDHAC2):c.1067T>G (p.Val356Gly)	PCDHA5, PCDHA1 +14 more (V356G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2325650	NM_018898.5(PCDHAC1):c.2224A>G (p.Ile742Val)	PCDHA9, PCDHA5 +13 more (I742V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2325549	NM_018904.3(PCDHA13):c.1000T>C (p.Cys334Arg)	PCDHA10, PCDHA13 +12 more (C334R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2325297	NM_018904.3(PCDHA13):c.757G>A (p.Glu253Lys)	PCDHA5, PCDHA10 +12 more (E253K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2310990	NM_018898.5(PCDHAC1):c.1649A>G (p.Asp550Gly)	PCDHA6, PCDHA4 +13 more (D550G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2305638	NM_018898.5(PCDHAC1):c.2043C>G (p.Asn681Lys)	PCDHA3, PCDHA6 +13 more (N681K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2304757	NM_018898.5(PCDHAC1):c.106G>T (p.Val36Leu)	PCDHA11, PCDHA4 +13 more (V36L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2302607	NM_018904.3(PCDHA13):c.4C>G (p.Leu2Val)	PCDHA13, PCDHA5 +12 more (L2V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2292341	NM_018899.6(PCDHAC2):c.406G>A (p.Val136Met)	PCDHA11, PCDHA1 +14 more (V136M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2292097	NM_018904.3(PCDHA13):c.1292G>A (p.Gly431Asp)	PCDHA11, PCDHA8 +12 more (G431D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2291606	NM_018904.3(PCDHA13):c.1522G>A (p.Val508Met)	PCDHA6, PCDHA4 +12 more (V508M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2289776	NM_018898.5(PCDHAC1):c.1204C>A (p.Pro402Thr)	PCDHA8, PCDHA9 +13 more (P402T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2282996	NM_018898.5(PCDHAC1):c.143C>A (p.Ala48Asp)	PCDHA4, PCDHA9 +13 more (A48D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2282337	NM_018898.5(PCDHAC1):c.778C>A (p.Pro260Thr)	PCDHA13, PCDHA6 +13 more (P260T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2281920	NM_018899.6(PCDHAC2):c.1195A>C (p.Lys399Gln)	PCDHA@, PCDHA11 +14 more (K399Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2277523	NM_018898.5(PCDHAC1):c.881A>G (p.Gln294Arg)	PCDHA10, PCDHA7 +13 more (Q294R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2274541	NM_018898.5(PCDHAC1):c.1748T>C (p.Val583Ala)	PCDHA10, PCDHA9 +13 more (V583A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2271141	NM_018899.6(PCDHAC2):c.1904T>C (p.Val635Ala)	PCDHAC1, PCDHA12 +14 more (V635A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2265265	NM_018904.3(PCDHA13):c.2192C>G (p.Ala731Gly)	PCDHA1, PCDHA10 +12 more (A731G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2251074	NM_018898.5(PCDHAC1):c.535G>A (p.Gly179Ser)	PCDHA3, PCDHA4 +13 more (G179S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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