ClinVar for Gene (Select 23022) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3226847	NM_001166108.2(PALLD):c.984C>T (p.Thr328=)	PALLD	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3226846	NM_001166108.2(PALLD):c.979C>A (p.His327Asn)	PALLD (H327N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3226845	NM_001166108.2(PALLD):c.954A>G (p.Gln318=)	PALLD	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3226843	NM_001166108.2(PALLD):c.878G>C (p.Arg293Thr)	PALLD (R293T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226842	NM_001166108.2(PALLD):c.847G>T (p.Ala283Ser)	PALLD (A283S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226841	NM_001166108.2(PALLD):c.815G>T (p.Arg272Leu)	PALLD (R272L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226840	NM_001166108.2(PALLD):c.811C>G (p.Pro271Ala)	PALLD (P271A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226839	NM_001166108.2(PALLD):c.797A>G (p.His266Arg)	PALLD (H266R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226837	NM_001166108.2(PALLD):c.765C>G (p.Arg255=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226835	NM_001166108.2(PALLD):c.712G>A (p.Gly238Arg)	PALLD (G238R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226834	NM_001166108.2(PALLD):c.692A>G (p.Glu231Gly)	PALLD (E231G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226833	NM_001166108.2(PALLD):c.688A>G (p.Met230Val)	PALLD (M230V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226832	NM_001166108.2(PALLD):c.630G>C (p.Gln210His)	PALLD (Q210H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226831	NM_001166108.2(PALLD):c.616T>C (p.Ser206Pro)	PALLD (S206P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226830	NM_001166108.2(PALLD):c.615G>C (p.Leu205=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226829	NM_001166108.2(PALLD):c.582T>C (p.Asn194=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226828	NM_001166108.2(PALLD):c.582T>A (p.Asn194Lys)	PALLD (N194K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226827	NM_001166108.2(PALLD):c.579A>G (p.Pro193=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226826	NM_001166108.2(PALLD):c.573A>T (p.Arg191Ser)	PALLD (R191S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226825	NM_001166108.2(PALLD):c.564A>G (p.Pro188=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226824	NM_001166108.2(PALLD):c.514G>T (p.Ala172Ser)	PALLD (A172S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226823	NM_001166108.2(PALLD):c.514G>A (p.Ala172Thr)	PALLD (A172T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226822	NM_001166108.2(PALLD):c.504G>A (p.Leu168=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226821	NM_001166108.2(PALLD):c.500A>G (p.Gln167Arg)	PALLD (Q167R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226820	NM_001166108.2(PALLD):c.490C>A (p.Pro164Thr)	PALLD (P164T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226819	NM_001166108.2(PALLD):c.48C>A (p.Asp16Glu)	PALLD (D16E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226818	NM_001166108.2(PALLD):c.469C>T (p.Pro157Ser)	PALLD (P157S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226817	NM_001166108.2(PALLD):c.460C>T (p.Pro154Ser)	PALLD (P154S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226816	NM_001166108.2(PALLD):c.446G>A (p.Ser149Asn)	PALLD (S149N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3226815	NM_001166108.2(PALLD):c.438A>G (p.Lys146=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226814	NM_001166108.2(PALLD):c.430G>A (p.Gly144Ser)	PALLD (G144S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226813	NM_001166108.2(PALLD):c.386C>T (p.Thr129Ile)	PALLD (T129I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226812	NM_001166108.2(PALLD):c.386C>A (p.Thr129Asn)	PALLD (T129N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226810	NM_001166108.2(PALLD):c.366T>A (p.Pro122=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226809	NM_001166108.2(PALLD):c.351T>G (p.Val117=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226808	NM_001166108.2(PALLD):c.346C>G (p.Pro116Ala)	PALLD (P116A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226807	NM_001166108.2(PALLD):c.3326T>C (p.Ile1109Thr)	CBR4, PALLD (I1092T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226806	NM_001166108.2(PALLD):c.3309C>T (p.Ala1103=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226805	NM_001166108.2(PALLD):c.323A>T (p.Lys108Ile)	PALLD (K108I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226804	NM_001166108.2(PALLD):c.3287C>G (p.Ala1096Gly)	CBR4, PALLD (A1079G +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226803	NM_001166108.2(PALLD):c.322A>G (p.Lys108Glu)	PALLD (K108E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3226802	NM_001166108.2(PALLD):c.3254G>T (p.Cys1085Phe)	CBR4, PALLD (C1068F +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226801	NM_001166108.2(PALLD):c.3253T>C (p.Cys1085Arg)	CBR4, PALLD (C1068R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226800	NM_001166108.2(PALLD):c.317C>T (p.Ala106Val)	PALLD (A106V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226798	NM_001166108.2(PALLD):c.3165A>T (p.Pro1055=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226794	NM_001166108.2(PALLD):c.3020C>G (p.Ala1007Gly)	CBR4, PALLD (A1007G +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226793	NM_001166108.2(PALLD):c.2950C>T (p.His984Tyr)	CBR4, PALLD (H260Y +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226792	NM_001166108.2(PALLD):c.288T>C (p.Asp96=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226791	NM_001166108.2(PALLD):c.2929C>T (p.Leu977=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226790	NM_001166108.2(PALLD):c.2915G>A (p.Ser972Asn)	CBR4, PALLD (S248N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226789	NM_001166108.2(PALLD):c.2902G>T (p.Val968Leu)	CBR4, PALLD (V244L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226788	NM_001166108.2(PALLD):c.2896A>C (p.Lys966Gln)	CBR4, PALLD (K242Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226787	NM_001166108.2(PALLD):c.2888T>C (p.Leu963Pro)	CBR4, PALLD (L239P +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226786	NM_001166108.2(PALLD):c.2887C>T (p.Leu963=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226785	NM_001166108.2(PALLD):c.27C>G (p.Ser9=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226784	NM_001166108.2(PALLD):c.2813C>T (p.Thr938Ile)	CBR4, PALLD (T214I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226783	NM_001166108.2(PALLD):c.2709T>C (p.His903=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226782	NM_001166108.2(PALLD):c.2683C>A (p.Pro895Thr)	CBR4, PALLD (P171T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226781	NM_001166108.2(PALLD):c.2675G>T (p.Gly892Val)	CBR4, PALLD (G168V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226780	NM_001166108.2(PALLD):c.2672G>C (p.Arg891Thr)	CBR4, PALLD (R167T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226778	NM_001166108.2(PALLD):c.2621A>C (p.Gln874Pro)	CBR4, PALLD (Q150P +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226777	NM_001166108.2(PALLD):c.2595T>G (p.Asn865Lys)	CBR4, PALLD (N141K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226776	NM_001166108.2(PALLD):c.2526C>T (p.Thr842=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226775	NM_001166108.2(PALLD):c.2508A>G (p.Pro836=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226772	NM_001166108.2(PALLD):c.2391G>A (p.Glu797=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226771	NM_001166108.2(PALLD):c.2369A>G (p.Asn790Ser)	CBR4, PALLD (N286S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226769	NM_001166108.2(PALLD):c.2315C>G (p.Ser772Cys)	CBR4, PALLD (S268C +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226768	NM_001166108.2(PALLD):c.2261T>C (p.Val754Ala)	CBR4, PALLD (V250A +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226767	NM_001166108.2(PALLD):c.2159T>C (p.Val720Ala)	CBR4, PALLD (V13A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226765	NM_001166108.2(PALLD):c.2087A>G (p.Asn696Ser)	PALLD (N209S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3226764	NM_001166108.2(PALLD):c.2076G>A (p.Glu692=)	PALLD	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3226763	NM_001166108.2(PALLD):c.2027C>G (p.Thr676Arg)	PALLD (T189R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3226762	NM_001166108.2(PALLD):c.2010T>A (p.Asp670Glu)	PALLD (D183E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3226761	NM_001166108.2(PALLD):c.1979A>C (p.Lys660Thr)	PALLD (K173T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3226759	NM_001166108.2(PALLD):c.195G>T (p.Ser65=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226758	NM_001166108.2(PALLD):c.1947G>A (p.Leu649=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226757	NM_001166108.2(PALLD):c.1893A>G (p.Lys631=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226756	NM_001166108.2(PALLD):c.1869T>A (p.Ile623=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226755	NM_001166108.2(PALLD):c.1785C>T (p.Ser595=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226754	NM_001166108.2(PALLD):c.172T>A (p.Phe58Ile)	PALLD (F58I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226753	NM_001166108.2(PALLD):c.1723G>C (p.Glu575Gln)	PALLD (E193Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226751	NM_001166108.2(PALLD):c.1693C>T (p.Pro565Ser)	PALLD (P183S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226750	NM_001166108.2(PALLD):c.1655G>A (p.Gly552Glu)	PALLD (G170E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226749	NM_001166108.2(PALLD):c.1651A>T (p.Met551Leu)	PALLD (M169L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226748	NM_001166108.2(PALLD):c.1637G>C (p.Cys546Ser)	PALLD (C164S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226747	NM_001166108.2(PALLD):c.1614C>A (p.Val538=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226746	NM_001166108.2(PALLD):c.1609G>T (p.Val537Phe)	PALLD (V155F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226745	NM_001166108.2(PALLD):c.1597A>G (p.Thr533Ala)	PALLD (T151A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226744	NM_001166108.2(PALLD):c.1597A>C (p.Thr533Pro)	PALLD (T151P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226742	NM_001166108.2(PALLD):c.154G>T (p.Asp52Tyr)	PALLD (D52Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226741	NM_001166108.2(PALLD):c.154G>C (p.Asp52His)	PALLD (D52H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226740	NM_001166108.2(PALLD):c.1518A>G (p.Leu506=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226739	NM_001166108.2(PALLD):c.1502A>G (p.Glu501Gly)	PALLD (E119G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226738	NM_001166108.2(PALLD):c.1472A>C (p.Gln491Pro)	PALLD (Q109P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226737	NM_001166108.2(PALLD):c.1470A>G (p.Leu490=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226736	NM_001166108.2(PALLD):c.145G>A (p.Ala49Thr)	PALLD (A49T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226734	NM_001166108.2(PALLD):c.139C>A (p.Arg47=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226733	NM_001166108.2(PALLD):c.138C>A (p.Ala46=)	PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226732	NM_001166108.2(PALLD):c.1364G>A (p.Gly455Asp)	PALLD (G455D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226731	NM_001166108.2(PALLD):c.1358C>G (p.Ala453Gly)	PALLD (A453G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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