Related gene-specific medical variations for Gene (Select 56126) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3304793	NM_018930.4(PCDHB10):c.1262T>C (p.Ile421Thr)	PCDHB10, PCDHB@ (I421T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304792	NM_018930.4(PCDHB10):c.1642C>A (p.Arg548Ser)	PCDHB10, PCDHB@ (R548S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304791	NM_018930.4(PCDHB10):c.1093C>G (p.Leu365Val)	PCDHB10, PCDHB@ (L365V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304790	NM_018930.4(PCDHB10):c.581T>G (p.Leu194Arg)	PCDHB10, PCDHB@ (L194R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304789	NM_018930.4(PCDHB10):c.353G>C (p.Arg118Pro)	PCDHB10, PCDHB@ (R118P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304788	NM_018930.4(PCDHB10):c.1270A>G (p.Thr424Ala)	PCDHB10, PCDHB@ (T424A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304787	NM_018930.4(PCDHB10):c.523A>G (p.Asn175Asp)	PCDHB10, PCDHB@ (N175D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304786	NM_018930.4(PCDHB10):c.322A>T (p.Ile108Phe)	PCDHB10, PCDHB@ (I108F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304785	NM_018930.4(PCDHB10):c.1384G>C (p.Glu462Gln)	PCDHB10, PCDHB@ (E462Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304784	NM_018930.4(PCDHB10):c.1648C>G (p.Leu550Val)	PCDHB10, PCDHB@ (L550V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304783	NM_018930.4(PCDHB10):c.2220C>G (p.Asp740Glu)	PCDHB10, PCDHB@ (D740E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304782	NM_018930.4(PCDHB10):c.1495C>T (p.Pro499Ser)	PCDHB10, PCDHB@ (P499S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304781	NM_018930.4(PCDHB10):c.2035G>T (p.Ala679Ser)	PCDHB10, PCDHB@ (A679S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304780	NM_018930.4(PCDHB10):c.733G>A (p.Ala245Thr)	PCDHB10, PCDHB@ (A245T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209576	NM_018930.4(PCDHB10):c.980T>C (p.Leu327Pro)	PCDHB10, PCDHB@ (L327P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209575	NM_018930.4(PCDHB10):c.940T>A (p.Ser314Thr)	PCDHB10, PCDHB@ (S314T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209574	NM_018930.4(PCDHB10):c.869C>G (p.Thr290Arg)	PCDHB10, PCDHB@ (T290R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209573	NM_018930.4(PCDHB10):c.805G>A (p.Val269Ile)	PCDHB10, PCDHB@ (V269I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3209572	NM_018930.4(PCDHB10):c.701A>C (p.Asp234Ala)	PCDHB10, PCDHB@ (D234A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209571	NM_018930.4(PCDHB10):c.578A>T (p.Glu193Val)	PCDHB10, PCDHB@ (E193V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209570	NM_018930.4(PCDHB10):c.563G>C (p.Gly188Ala)	PCDHB10, PCDHB@ (G188A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209569	NM_018930.4(PCDHB10):c.524A>G (p.Asn175Ser)	PCDHB10, PCDHB@ (N175S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209568	NM_018930.4(PCDHB10):c.372G>T (p.Arg124Ser)	PCDHB10, PCDHB@ (R124S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209567	NM_018930.4(PCDHB10):c.2369C>G (p.Thr790Ser)	PCDHB10, PCDHB@ (T790S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209566	NM_018930.4(PCDHB10):c.2368A>T (p.Thr790Ser)	PCDHB10, PCDHB@ (T790S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209565	NM_018930.4(PCDHB10):c.2317A>G (p.Ile773Val)	PCDHB10, PCDHB@ (I773V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209563	NM_018930.4(PCDHB10):c.2134G>T (p.Ala712Ser)	PCDHB10, PCDHB@ (A712S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209562	NM_018930.4(PCDHB10):c.2119G>T (p.Val707Leu)	PCDHB10, PCDHB@ (V707L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209560	NM_018930.4(PCDHB10):c.1823A>T (p.Lys608Met)	PCDHB10, PCDHB@ (K608M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209559	NM_018930.4(PCDHB10):c.1760C>T (p.Thr587Ile)	PCDHB10, PCDHB@ (T587I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209557	NM_018930.4(PCDHB10):c.1478C>A (p.Pro493His)	PCDHB10, PCDHB@ (P493H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209556	NM_018930.4(PCDHB10):c.1468C>A (p.Leu490Met)	PCDHB10, PCDHB@ (L490M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209555	NM_018930.4(PCDHB10):c.1403T>A (p.Leu468Gln)	PCDHB10, PCDHB@ (L468Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209554	NM_018930.4(PCDHB10):c.1361C>T (p.Thr454Ile)	PCDHB10, PCDHB@ (T454I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209553	NM_018930.4(PCDHB10):c.1223C>T (p.Ala408Val)	PCDHB10, PCDHB@ (A408V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209552	NM_018930.4(PCDHB10):c.1153A>G (p.Ile385Val)	PCDHB10, PCDHB@ (I385V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209551	NM_018930.4(PCDHB10):c.1034C>T (p.Pro345Leu)	PCDHB10, PCDHB@ (P345L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655829	NM_018930.4(PCDHB10):c.1905A>G (p.Ala635=)	PCDHB@, PCDHB10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2623803	NM_018930.4(PCDHB10):c.76G>A (p.Ala26Thr)	PCDHB10, PCDHB@ (A26T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620723	NM_018930.4(PCDHB10):c.1031C>G (p.Pro344Arg)	PCDHB10, PCDHB@ (P344R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596936	NM_018930.4(PCDHB10):c.1329C>A (p.Asp443Glu)	PCDHB10, PCDHB@ (D443E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591877	NM_018930.4(PCDHB10):c.1031C>A (p.Pro344His)	PCDHB10, PCDHB@ (P344H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554262	NM_018930.4(PCDHB10):c.2257T>C (p.Tyr753His)	PCDHB10, PCDHB@ (Y753H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552420	NM_018930.4(PCDHB10):c.476A>T (p.Asp159Val)	PCDHB10, PCDHB@ (D159V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2552236	NM_018930.4(PCDHB10):c.724T>C (p.Phe242Leu)	PCDHB10, PCDHB@ (F242L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545911	NM_018930.4(PCDHB10):c.1520A>G (p.Asn507Ser)	PCDHB10, PCDHB@ (N507S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543755	NM_018930.4(PCDHB10):c.458G>A (p.Arg153Lys)	PCDHB10, PCDHB@ (R153K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538764	NM_018930.4(PCDHB10):c.120G>C (p.Glu40Asp)	PCDHB10, PCDHB@ (E40D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535086	NM_018930.4(PCDHB10):c.1711C>T (p.Pro571Ser)	PCDHB10, PCDHB@ (P571S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532741	NM_018930.4(PCDHB10):c.1690C>T (p.Pro564Ser)	PCDHB10, PCDHB@ (P564S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532493	NM_018930.4(PCDHB10):c.332A>G (p.Asp111Gly)	PCDHB10, PCDHB@ (D111G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527652	NM_018930.4(PCDHB10):c.664A>G (p.Arg222Gly)	PCDHB10, PCDHB@ (R222G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493874	NM_018930.4(PCDHB10):c.1916G>A (p.Arg639Lys)	PCDHB10, PCDHB@ (R639K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488060	NM_018930.4(PCDHB10):c.821A>G (p.Asn274Ser)	PCDHB10, PCDHB@ (N274S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480384	NM_018930.4(PCDHB10):c.1298C>G (p.Thr433Ser)	PCDHB10, PCDHB@ (T433S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478280	NM_018930.4(PCDHB10):c.1885C>A (p.Leu629Met)	PCDHB10, PCDHB@ (L629M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477601	NM_018930.4(PCDHB10):c.607G>C (p.Glu203Gln)	PCDHB10, PCDHB@ (E203Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477430	NM_018930.4(PCDHB10):c.1475C>T (p.Pro492Leu)	PCDHB10, PCDHB@ (P492L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469771	NM_018930.4(PCDHB10):c.331G>T (p.Asp111Tyr)	PCDHB10, PCDHB@ (D111Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467880	NM_018930.4(PCDHB10):c.682G>A (p.Val228Ile)	PCDHB10, PCDHB@ (V228I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2466857	NM_018930.4(PCDHB10):c.2237C>A (p.Thr746Asn)	PCDHB10, PCDHB@ (T746N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457731	NM_018930.4(PCDHB10):c.704T>C (p.Val235Ala)	PCDHB10, PCDHB@ (V235A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455695	NM_018930.4(PCDHB10):c.631A>C (p.Thr211Pro)	PCDHB10, PCDHB@ (T211P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410627	NM_018930.4(PCDHB10):c.1660G>A (p.Ala554Thr)	PCDHB10, PCDHB@ (A554T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410482	NM_018930.4(PCDHB10):c.1601C>T (p.Thr534Ile)	PCDHB10, PCDHB@ (T534I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404066	NM_018930.4(PCDHB10):c.2260G>A (p.Glu754Lys)	PCDHB10, PCDHB@ (E754K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402969	NM_018930.4(PCDHB10):c.1651G>A (p.Val551Met)	PCDHB10, PCDHB@ (V551M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395514	NM_018930.4(PCDHB10):c.686G>T (p.Arg229Leu)	PCDHB10, PCDHB@ (R229L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394071	NM_018930.4(PCDHB10):c.1645G>A (p.Val549Met)	PCDHB10, PCDHB@ (V549M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387393	NM_018930.4(PCDHB10):c.556G>A (p.Asp186Asn)	PCDHB10, PCDHB@ (D186N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377484	NM_018930.4(PCDHB10):c.617G>A (p.Gly206Glu)	PCDHB10, PCDHB@ (G206E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366815	NM_018930.4(PCDHB10):c.61T>G (p.Trp21Gly)	PCDHB10, PCDHB@ (W21G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2362836	NM_018930.4(PCDHB10):c.1329C>G (p.Asp443Glu)	PCDHB10, PCDHB@ (D443E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361034	NM_018930.4(PCDHB10):c.430G>C (p.Glu144Gln)	PCDHB10, PCDHB@ (E144Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352892	NM_018930.4(PCDHB10):c.845T>C (p.Phe282Ser)	PCDHB10, PCDHB@ (F282S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347351	NM_018930.4(PCDHB10):c.2149A>G (p.Arg717Gly)	PCDHB10, PCDHB@ (R717G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345303	NM_018930.4(PCDHB10):c.1576G>T (p.Ala526Ser)	PCDHB10, PCDHB@ (A526S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342374	NM_018930.4(PCDHB10):c.1022A>G (p.Asn341Ser)	PCDHB10, PCDHB@ (N341S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342230	NM_018930.4(PCDHB10):c.1928T>C (p.Leu643Pro)	PCDHB10, PCDHB@ (L643P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327862	NM_018930.4(PCDHB10):c.178G>A (p.Ala60Thr)	PCDHB10, PCDHB@ (A60T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324086	NM_018930.4(PCDHB10):c.1045G>T (p.Val349Leu)	PCDHB10, PCDHB@ (V349L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313059	NM_018930.4(PCDHB10):c.514A>C (p.Ile172Leu)	PCDHB10, PCDHB@ (I172L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310556	NM_018930.4(PCDHB10):c.213C>A (p.Asn71Lys)	PCDHB10, PCDHB@ (N71K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310501	NM_018930.4(PCDHB10):c.2224A>G (p.Arg742Gly)	PCDHB10, PCDHB@ (R742G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307174	NM_018930.4(PCDHB10):c.1955G>T (p.Arg652Leu)	PCDHB10, PCDHB@ (R652L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2303791	NM_018930.4(PCDHB10):c.581T>C (p.Leu194Pro)	PCDHB10, PCDHB@ (L194P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300272	NM_018930.4(PCDHB10):c.1168C>T (p.Pro390Ser)	PCDHB10, PCDHB@ (P390S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295582	NM_018930.4(PCDHB10):c.1964C>G (p.Thr655Ser)	PCDHB10, PCDHB@ (T655S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2293660	NM_018930.4(PCDHB10):c.1189G>C (p.Val397Leu)	PCDHB10, PCDHB@ (V397L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274665	NM_018930.4(PCDHB10):c.715G>A (p.Ala239Thr)	PCDHB10, PCDHB@ (A239T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265625	NM_018930.4(PCDHB10):c.683T>C (p.Val228Ala)	PCDHB10, PCDHB@ (V228A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252822	NM_018930.4(PCDHB10):c.1921G>C (p.Val641Leu)	PCDHB10, PCDHB@ (V641L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2242159	NM_018930.4(PCDHB10):c.1522G>C (p.Ala508Pro)	PCDHB10, PCDHB@ (A508P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238868	NM_018930.4(PCDHB10):c.1538T>G (p.Leu513Arg)	PCDHB10, PCDHB@ (L513R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234152	NM_018930.4(PCDHB10):c.1342G>A (p.Ala448Thr)	PCDHB10, PCDHB@ (A448T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220256	NM_018930.4(PCDHB10):c.1199T>C (p.Phe400Ser)	PCDHB10, PCDHB@ (F400S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215987	NM_018930.4(PCDHB10):c.1886T>C (p.Leu629Pro)	PCDHB10, PCDHB@ (L629P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214754	NM_018930.4(PCDHB10):c.863T>C (p.Ile288Thr)	PCDHB10, PCDHB@ (I288T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209753	NM_018930.4(PCDHB10):c.520C>T (p.Pro174Ser)	PCDHB10, PCDHB@ (P174S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208407	NM_018930.4(PCDHB10):c.1411G>A (p.Gly471Ser)	PCDHB10, PCDHB@ (G471S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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